Immunostimulatory oligonucleotides and uses thereof

ABSTRACT

Oligonucleotides containing the non-palindromic sequence motif:  
     X 1 X 2 X 3 X 4 X 5 X 6 X 7 X 8 ,  
     wherein X, is C,T,G or A (preferably T or C); wherein X 2  is C,T,G or A; wherein X 7  is C,T,G or A (preferably G); at least three, and preferably all, of X 3 , X 4 , X 5 , X 6  and X 8  are T; and with the proviso that, in the motif, a C does not precede a G (in other terms, the nucleic acid motif does not consist of a CpG oligonucleotide), that modulate the immune response of animals of the order Primate, including humans, are disclosed. This immune modulation is characterized by stimulation of proliferation, differentiation, cytokine production and antibody production on B-cells and cell differentiation on plasmacytoid dendritic cells.

FIELD OF THE INVENTION

[0001] The present invention relates generally to oligonucleotides containing the non-palindromic sequence motif:

X₁X₂X₃X₄X₅X₆X₇X₈,

[0002] wherein X₁ is C,T,G or A (preferably T or C); X₂ is C,T,G or A; X₇ is C,T,G or A (preferably G); at least three, and preferably all, of X₃, X₄, X₅, X₆ and X₈ are T; with the proviso that, in the motif, a C does not precede a G, that are immunostimulatory in animals of the order Primate, including humans.

[0003] Relevant References

[0004] Patent Documents

[0005] U.S. Pat. No. 5,663,153

[0006] U.S. Pat. No. 5,723,335

[0007] U.S. Pat. No. 6,090,791

[0008] U.S. Pat. No. 6,194,388

[0009] U.S. Pat. No. 6,207,646

[0010] U.S. Pat. No. 6,239,116

[0011] U.S. Pat. No. 6,429,199

[0012] EP 0468520

[0013] WO 95/26204

[0014] WO 96/02555

[0015] WO 98/40100

[0016] WO 98/52962

[0017] WO 99/33488

[0018] WO 99/56755

[0019] WO 00/62802

[0020] WO 01/00231

[0021] WO 01/00232

[0022] WO 01/55370

[0023] Other References

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[0070] Krieg A M et al., Oligodeoxynucleotide modifications determine the magnitude of B cell stimulation by CpG motifs. Antisense Nucleic Acid Drug Dev 6(2):133-9, Summer 1996.

[0071] Tokunaga T et al., A synthetic single-stranded DNA, poly(dG,dC), induces interferon-alpha/beta and -gamma, augments natural killer activity, and suppresses tumor growth. Jpn J Cancer Res 79:682-6, June 1988.

[0072] Yi A K et al., Rapid immune activation by CpG motifs in bacterial DNA. Systemic induction of IL-6 transcription through an antioxidant-sensitive pathway. J Immunol 157:5394-402, Dec. 15, 1996.

[0073] Lipford G B et al., CpG-containing synthetic oligonucleotides promote B and cytotoxic T cell responses to protein antigen: a new class of vaccine adjuvants. Eur J Immunol 27:2340-2344.1997.

[0074] Lipford G B et al., Immunostimulatory DNA: sequence-dependent production of potentially harmful or useful cytokines. Eur J Immunol 27:3420-3426, (1997).

[0075] Rankin R et al., CpG motif identification for veterinary and laboratory species demonstrates that sequence recognition is highly concerved. Antisence Nucleic Acid Drug Dev 11:333-340 (2001).

[0076] Decker T et al., ImmunostimulatoryCpG-oligonucleotides induce functional high affinity IL-2 receptors on B-CLL cells: costimulation with IL-2 results in a highly immunogenic phenotype. Exp Hematol 28:558-568 (2000).

[0077] Decker T and Peschel C, Effect of immunostimulatory CpG-oligonucleotides in chronic lymphocytic leukemia B cells. Leuk Lymphoma 42:301-307 (2001).

[0078] Jahrsdorfer B et al., CpG DNA increases primary malignant B cell expression of costimulatory molecules and target antigens. J Leukoc Biol 69:81-88 (2001).

[0079] Krieg A M. GpG motifs in bacterial DNA and their immune effects. Annu. Rev. Immunol. 20, 709-760, (2002)

[0080] Kadowaki N, Antonenko S, Liu Y J. Distinct CpG DNA and polyinosinic-polycytidylic acid double-stranded RNA, respectively, stimulate CD11c⁻ type 2 dendritic cell precursors and CD11c⁺ dendritic cells to produce type I IFN. J. Immunol, 166, 2291- 2295, (2001).

[0081] Krug A, Rothenfusser S, Hormung V, Jahrsdorfer B, Blackwell S, Ballas Z K, Endres S, Krieg A M, Hartmann G. Identification of CpG oligonucleotide sequences with high induction of IFN-α/β in plasmacytoid dendritic cells. Eur. J. Immunol. 31, 2154-2163, (2001).

[0082] Krug A, Towarowski A, Britsch S, Rothenfusser S, Hornung V, Bals R, Giese T, Engelmann H, Endres S, Krieg A M, Hartmann G. Toll-like receptor expression reveals CpG DNA as a unique microbial stimulus for plasmacytoid dendritic cells which synergizes with CD40 ligand to induce high amounts of IL-12. Eur J Immunol. 31, 3026-3037, 2001.

[0083] Hartmann G, Krieg A M. Mechanism and function of a newly identified CpG DNA motif in human primary B cells. J. Immunol.164, 944-952, (2000).

[0084] Chace J H, Hooker N A, Mildenstein K L, Krieg A M, Chowdery J S. Bacterial DNA-induced NK cell IFNγ production is dependent on macrophage secretion of IL-12. Clin. Immunol. Immunopathol. 84, 185-193, (1997).

[0085] Sparwasser T, Koch E S, Vabulas R M, Heeg K, Lipford G B, Ellwart J W, Wagner. Bacterial DNA and immunostimulatory CpG oligodeoxynucleotides trigger maturation and activation of murine dendritic cells. Eur. J. Immunol. 28, 2045-2054, 1998.

[0086] Ballas Z K, Rasmussen W L, Krieg A M. Induction of natural killer activity in murine and human cells by CpG motifs in oligodeoxynucleotides and bacterial DNA. J. Immunol. 157, 1840-1845, (1996).

[0087] Hornung V, Rothenfusser S, Britsch S, Krug A, Jahrsdorfer B, Giese T, Endres S, Hartmann G. Quantitative expression of toll-like receptor 1-10 mRNA in cellular subsets of human peripheral blood mononuclear cells and sensitivity to CpG oligodeoxynucleotides. J Immunol. 168, 4531-4537, (2002).

[0088] Lipford G B, Bauer M, Blank C, Reiter R, Wagner H, Heeg K. CpG-containing synthetic oligodeoxynucleotides promote B and cytotoxic T cell responses to protein antigen: A new class of vaccine adjuvants. Eur. J. Immunol. 27, 2340-2344, (1997).

[0089] Chu R S, Targoni O S, Krieg A M, Lehman P V, Harding C V. CpG oligodeoxynucleotides act as adjuvants that switch on T helper 1 (Th1) immunity. J. Exp. Med. 186, 1623-1631, (1997).

[0090] Moldovenu G J, Love-Homan L, Huang W Q, Krieg A M. CpG DNA, a novel immune enhancer for systemic and mucosal immunization with influenza virus. Vaccine.16, 1216-1224, (1998).

[0091] Davis H L, Weeratna R, Waldschmidt T J, Tygrett L, Schorr J, Krieg A M. CpG DNA is a potent enhancer of specific immunity in mice immunized with recombinant hepatitis B surface antigen. J. Immunol.160, 870-876, (1998).

[0092] Weeratna R, McCluskie M J, Yu X, Davis H L. CpG DNA induces stronger immune responses with less toxicity than other adjuvants. Vaccine. 18, 1755-1762, (2000).

[0093] Kline J N, Businga T R, Waldschmidt T J, Weinstock J V, Krieg A M. Modulation of airway inflammation by CpG oligodeoxynucleotides in a murine model of asthma. J. Immunol. 15, 2555-2559, (1998).

[0094] Magone, M T, Chan C C, Beck L, Whitcup S M, Raz E. Systemic or mucosal administration of immunostimulatory DNA inhibits early and late phases of murine allergic conjunctivitis. Eur. J. Immunol. 30, 1841-1850, (2000).

[0095] Wooldridge J E, Ballas Z, K, Krieg A M, Weiner G J. Immunostimulatory oligodeoxynucleotides containing CpG motifs enhance the efficacy of monoclonal antibody therapy of lymphoma. Blood. 89, 2994-2998, (1997).

[0096] Carpentier, A F, Chen L, Maltoni F, Delattre J Y. Oligodeoxynucleotides containing CpG motifs can induce rejection of a neuroblastoma in mice. Cancer Res. 59, 5429-5432, (1999).

[0097] Hartmann G, Weeratna R, Ballas Z K, Payette P, Suparto, I, Rasmussen W L, Wadschmidt M, Sajuthi D, Purcells R H, Davis H L, Krieg A M. Delineation of a CpG phosphorothioate oligodeoxynucleotide for activating primate immune responses in vitro and in vivo. J. Immunol.164, 1617-1624, (2000).

[0098] Rankin R, Pontarollo R, Ioannou X, Krieg A M, Hecker R, Babiuk L A, Van Drunen Littel-van Den Hurk S. CpG motif identification for veterinary and laboratory species demonstrates that sequence recognition is highly conserved. Antisense Nucleic Acid Drug Dev. 11, 333-340, (2001).

[0099] Verthelyi D, Ishii K J, Gursel M, Takeshita F, Klinman D M. Human peripheral blood cells differentially recognize and respond to two distinct CPG motifs. J Immunol. 166: 2372-2377, (2001).

[0100] Gursel M, Verthelyi D, Gursel I, Ishii K J, Klinman D M. Differential and competitive activation of human immune cells by distinct classes of CpG oligodeoxynucleotide. J Leukoc Biol.71: 813-820, (2002).

[0101] Yamamoto S, Yamamoto T, Kataoka T, Kuramoto E, Yano O, Tokunaga T. Unique palindromic sequences in synthetic oligodeoxynucleotides are required to induce IFN and augment IFN-mediated natural killer activity. J immunol 148, 4072-4076, (1992).

[0102] Liang H, Nishioka Y, Reich C F, Pisetsky D S, Lipsky P E. Activation of human B cells by phosphorothioate oligodeoxynucleotides. J. Clin. Invest. 98, 1119-1129, (1996).

[0103] Takeshita F, Leifer C A, Gursel I, Ishii K J, Takeshita S, Gursel M, Klinman D M. Cutting edge: Role of Toll-like receptor 9 in CpG DNA-induced activation of human cells. J Immunol. 67:3555-3558, (2001).

[0104] Bauer S, Kirschning C J, Hacker H, Redecke V, Hausmann S, Akira S, Wagner H, Lipford G B. Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition. Proc Natl Acad Sci USA. 98: 9237-9242, (2001).

[0105] Vollmer J, Janosch A, Laucht M, Ballas Z K, Schetter C, Krieg A M. Highly immunostimulatory CpG-free oligodeoxynucleotides for activation of human leukocytes. Antisense Nucleic Acid Drug Dev. 12:165-175, (2002).

[0106] Jahrsdorfer B, Jox R, Muhlenhoff L, Tschoep K, Krug A, Rothenfusser S, Meinhardt G, Emmerich B, Endres S, Hartmann G. Modulation of malignant B cell activation and apoptosis by bcl-2 antisense ODN and immunostimulatory CpG ODN. J Leukoc Biol. 72 :83-92 (2002)

[0107] Gursel M, Verthelyi D, Klinman D M. CpG oligodeoxynucleotides induce human monocytes to mature into functional dendritic cells. Eur J Immunol. 32 :2617-22 (2002).

[0108] Hornung V, Rothenfusser S, Britsch S, Krug A, Jahrsdorfer B, Giese T, Endres S, Hartmann G. Quantitative expression of toll-like receptor 1-10 mRNA in cellular subsets of human peripheral blood mononuclear cells and sensitivity to CpG oligodeoxynucleotides. J Immunol. 168:4531-7 (2002).

[0109] Krug A, Towarowski A, Britsch S, Rothenfusser S, Hornung V, Bals R, Giese T, Engelmann H, Endres S, Krieg A M, Hartmann G. Toll-like receptor expression reveals CpG DNA as a unique microbial stimulus for plasmacytoid dendritic cells which synergizes with CD40 ligand to induce high amounts of IL-12. Eur J Immunol. 31:3026-37 (2002).

[0110] Kadowaki N, Ho S, Antonenko S, Malefyt R W, Kastelein R A, Bazan F, Liu Y J. Subsets of human dendritic cell precursors express different toll-like receptors and respond to different microbial antigens. J Exp Med. 17;194:863-9 (2001).

[0111] Krug A, Rothenfusser S, Hornung V, Jahrsdorfer B, Blackwell S, Ballas Z K, Endres S, Krieg A M, Hartmann G. Identification of CpG oligonucleotide sequences with high induction of IFN-alpha/beta in plasmacytoid dendritic cells. Eur J Immunol. 31:2154-63 (2001).

[0112] Bauer M, Redecke V, Ellwart J W, Scherer B, Kremer J P, Wagner H, Lipford G B. Bacterial CpG-DNA triggers activation and maturation of human CD11c−, CD123+ dendritic cells. J Immunol. 166:5000-7 (2001).

[0113] Olbrich A R, Schimmer S, Heeg K, Schepers K, Schumacher T N, Dittmer U. Effective postexposure treatment of retrovirus-induced disease with immunostimulatory DNA containing CpG motifs. J Virol. 76:11397-404 (2002).

[0114] Decker T, Peschel C. Effect of immunostimulatory CpG-oligonucleotides in chronic lymphocytic leukemia B cells. Leuk Lymphoma. 42:301-7 (2001).

[0115] Decker T, Schneller F, Sparwasser T, Tretter T, Lipford G B, Wagner H, Peschel C. Immunostimulatory CpG-oligonucleotides cause proliferation, cytokine production, and an immunogenic phenotype in chronic lymphocytic leukemia B cells. Blood. 95:999-1006 (2000).

[0116] Decker T, Schneller F, Kronschnabl M, Dechow T, Lipford G B, Wagner H, Peschel C. Immunostimulatory CpG-oligonucleotides induce functional high affinity IL-2 receptors on B-CLL cells: costimulation with IL-2 results in a highly immunogenic phenotype. Exp Hematol. 28:558-68 (2000).

[0117] Jahrsdorfer B, Hartmann G, Racila E, Jackson W, Muhlenhoff L, Meinhardt G, Endres S, Link B K, Krieg A M, Weiner G J. CpG DNA increases primary malignant B cell expression of costimulatory molecules and target antigens. J Leukoc Biol.69:81-8 (2001).

[0118] Chen W, Yu Y, Shao C, Zhang M, Wang W, Zhang L, Cao X. Enhancement of antigen-presenting ability of B lymphoma cells by immunostimulatory CpG-oligonucleotides and anti-CD40 antibody. Immunol Lett. 77: 17-23 (2001).

BACKGROUND OF THE INVENTION

[0119] The Immune System

[0120] The major function of the immune system is to protect the host of invading pathogens. A number of different cell types, both antigen-independent and antigen-specific, have evolved to detect and neutralize these invading pathogens. Among them, lymphocytes have an important characteristic, which is their ability to specifically recognize antigens, a feature not possessed by any other cell. This means that any lymphocyte function stimulated by an antigen is directed solely at that antigen.

[0121] Lymphocytes may be divided into two major populations: T and B. T lymphocytes have a central role in regulating the immune response and for this they produce and secrete lymphokines (i.e.: interleukins). B-lymphocytes are the only cells that produce antibodies, which are proteins—Immunoglobulins (IgG)—that recognize and bind antigens.

[0122] Some T lymphocytes are known as helper (Th lymphocytes) because they assist B cells to produce antibody. T-lymphocytes express a characteristic membrane molecule designated CD4. Other T lymphocytes are known as cytotoxic (CTL) because they are capable of killing certain cells. They express a different characteristic membrane protein designated CD8.

[0123] Th lymphocytes, in mice, have been subdivided according to the lymphokines they produce in groups designated Th0, Th1 and Th2. In general, Th 1 lymphocytes produce lymphokines which stimulate macrophages and CTLS (IL2, IFNγ, TNF-β), Th 2 lymphocytes produce lymphokines which stimulate B lymphocytes to proliferate and produce antibody (IL 2, IL5, IL6, IL10, IL13), whilst Th 0 lymphocytes produce a mixture of lymphokines and are thought to be an intermediate stage from which Th 1 and Th 2 lymphocytes are derived. In humans, Th1 and Th2 like lymphocytes have been demonstrated, although they do seem to show a less strict division with respect to their patterns of cytokine secretion.

[0124] A third population of lymphocytes, which lack the major makers of T and B cells include the natural killer cells (NK cells), the killer cells (K cells) and the lymphokine-activated killer cells (L A K cells). NK cells can kill certain tumor cells and some virally infected cells, but unlike cytotoxic T lymphocytes they are not capable of recognizing a specific antigen. K cells are able to bind to cells, which have antibody to them via their antigen-binding regions and kill them. L A K cells do not specifically recognize an antigen but they are capable of destroying a wider range of targets a NK cells.

[0125] Macrophages and dendritic cells play a critical role in initiating immune responses, helping T cells to respond to antigens.

[0126] There are several antibody classes. The IgG class comprises most of the circulating antibodies and it has four subclasses designated IgG1, IgG2, IgG3 and IgG4.

[0127] The IgM class comprises about 10% of the circulating antibodies. These are the principal antibodies produce during the primary immunological response. The IgA class comprises most of the antibody secreted at mucous membranes and exerts its protective effect by blocking access of the antigen to the inner body. The IgD class comprises less than 1% of serum antibodies and its biological role is largely unknown. The IgE class comprises antibodies that are mainly bound to the surface of most cells and basophils. These antibodies are associated with reactions that occur in individuals who are undergoing allergic reactions.

[0128] Vaccines and Vaccines Adjuvants

[0129] Vaccines are preparations used to stimulate animals to mount an immune response against antigens included in the vaccine.

[0130] Vaccines often include adjuvants, which are substances that used in combination with specific antigen produce more immunity than the antigen used alone. (Ramon, G.,1926. Procedes pour accroite la production des antitoxins. Ann. Inst. Pasteur. 40, 1-10).

[0131] Many kind of compounds function as vaccine adjuvants (Edelman, R., 2000. An overview of adjuvant use, in: Vaccine Adjuvants. Preparation Methods and Research Protocols. D. T. O'Hagan, Ed., Humana Press, Totowa, N.J. References cited in this article are incorporated herein as background material). However, currently, the only adjuvants approved for use in humans are aluminum salts (Gupta, R. K. and Rost, B. E., 2000. Aluminum compounds as vaccine adjuvants in: Vaccine Adjuvants. Preparation Methods and Research Protocols. D. T. O'Hagan, Ed., Humana Press, Totowa, N.J.) and the oil-in-water emulsion M F 59 (Ott, G. Radhakrishman, R. Fang, J. and Hora, M., 2000. The adjuvant M F 59: A 10-Year Perspective, in : Vaccine Adjuvants. Preparation Methods and Research Protocols. D. T. O'Hagan, Ed., Humana Press, Totowa, N.J.).

[0132] Nucleic Acids as Immunostimulatory Compounds

[0133] Several polynucleotides have been demonstrated to have immunostimulatory properties. For example, poly (I, C) is an inducer of interferon (IFN) production, macrophage activation and NK cell activation (Talmadge, J. E., Adams, J., Phillips, H., Collins, M., Lenz, B., Schneider, M., Schlick, E., Ruffmann, R., Wiltrout, R. H., Chirigos, M. A. 1985. Immunomodulatory effects in mice of polyinosinic-polycytidylic acid complexed with poly-L:-lysine and carboxymethylcellulose. Cancer Res. 45:1058; Wiltrout, R. H., Salup, R. R., Twilley, T. A., Talmage, J. E. 1985. mmunomodulation of natural killer activity by polyribonucleotides. J. Biol. Resp. Mod. 4:512), poly (dG,dC) is mitogenic for B cells (Messina, J. P., Gilkerson, G. S., Pisetsky, D. S. 1993. The influence of DNA structure on the in vitro stimulation of murine lymphocytes by natural and synthetic polynucleotide antigens. Cell. Immunol. 147:148) and induces IFN and NK activity (Tocunaga, T., Yamamoto, S., Namba, K.1988. A synthetic single-stranded DNA, poly(dG,dC), induces interferon-α/β and -γ, augments natural killer activity, and suppresses tumor growth. Jpn.J. Cancer Res. 79:682).

[0134] Bacterial DNA has also been reported to have immunostimulatory properties. These properties include the induction of cytokines (interferon gamma (IFN γ), alpha (IFN α), beta (IFN β); tumor necrosis factor alpha (TNF α), interleukin 6 (IL6), 12 (IL 12) and 18 (IL 18), as well as the direct stimulation of B cells (Yamamoto, S. et al. 1988. In vitro augmentation of natural killer cell activity of interferon α/β and γ with deoxyribonucleic acid fraction from Mycobacterium bovis BCG. Jpn. J. Cancer Res. (Gann) 79: 866-873 ; Yamamoto S. et al, 1992. DNA from bacteria, but not from vertebrates, induces interferons, activates natural killer cells and inhibits tumor growth. Microbiol. Immunol. 36: 983-997.; Klinman, D. M., Yi, A -K., Beaucage, S. L., Conover, J. and Krieg, A. M., 1996.

[0135] CpG motifs present in bacterial DNA rapidly induce lymphocytes to secrete interleukin 6, interleukin 12 and interferon γ. Proc. Natl. Acad. Sci. USA 93, 2879-2883. Halpern, M. D., et al. 1996. Bacterial DNA induces murine interferon-γ production by stimulation of interleukin-12 and tumor necrosis factor-α. Cell. Immunol. 167: 72-78. Sparwasser, T. et al, 1997. Macrophages sense pathogens via DNA motifs: induction of tumor necrosis factor-α-mediated shock. Eur. J. Immunol. 27: 1671-1679; Krieg, A. M. et al., 1995. CpG motifs in bacterial DNA trigger direct B-cell activation. Nature 374: 345-349).

[0136] In contrast, it has been reported that mammalian DNA has no significant immune effects (Pisetsky, D. S. 1996. The immunologic properties of DNA. J. Immunol. 156: 421-423; Messina et al. 1991. Stimulation of in vitro murine lymphocyte proliferation by bacterial DNA. J. Immunol. 147: 1759).

[0137] Synthetic DNA has also been reported to be immunostimulatory if contains unmethylated CpG motifs. (Yamamoto, S et al.; 1992. Unique palindromic sequences in synthetic oligonucleotides are required to induce INF and augment INF-mediated natural killer activity. J. Immunol. 148: 4072-4076; Ballas, Z. K., et al.; 1996. Induction of NK activity in murine and human cells by CpG motifs in oligodeoxynucleotides and bacterial DNA. J. Immunol. 157: 1840-1845; Hartmann, G., Krieg, A. M. 2000. Mechanism and function of a newly identified CpG DNA motif in human primary B cells. J. Immunol. 164:944; Hartmann, G., Weeratna, R. D., Ballas, Z. K., Payette, P., Blackwell, S., Suparto, I., Rasmussen, W. L., Waldschmidt, M., Sajuthi, D., Purcell, R. H., Davis, H. L., Krieg, A. M. 2000. Delineation of a CpG phosphorothioate oligodeoxynucleotide for activating primate immune responses in vitro and in vivo. J. Immunol. 164:1617; Verthelyi, D., Ishii, K. J., Gursel, M., Takeshita, F., Klinman, D. M. 2001. Human peripheric blood cells differentially recognize and respond to two distinct CpG motifs. J. Immunol. 166:2372). However, one oligonucleotide containing phosphorothioate bonds that lack CpG motifs has been found to have some immunostimulatory activity on human B cells (Liang, H., Nishioka, Y., Reich, C. F., Pisetsky, D. S., Lipsky, P. E. 1996. Activation of human B cells by phosphorothioate oligonucleotides. J. Clin. Invest. 98:1119). This particular non-CpG oligonucleotide containing phosphorothioate bonds is a poy-T chain, 20 nucleotides long. Also, Vollmer et al (Vollmer J, Janosch A, Laucht M, Ballas Z K, Schetter C, Krieg A M. Highly immunostimulatory CpG-free oligodeoxynucleotides for activation of human leukocytes. Antisense Nucleic Acid Drug Dev. 12:165-175, 2002) reported immunostimulation by phosphorothioate poly T ODNs. These authors pointed out that poly T ODNs are only active as phosphorothioate ODNs and have much lower activity than CpG ODNs.

[0138] It has now been discovered that non-CpG oligonucleotides containing the following non-palindromic sequence motif:

X₁X₂X₃X₄X₅X₆X₇X₈,

[0139] wherein X₁ is C,T,G or A (preferably T or C); X₂ is C,T,G or A; X₇ is C,T,G or A (preferably G); at least three, and preferably all, of X₃, X₄, X₅, X₆ and X₈ are T; with the proviso that, in the motif, a C does not precede a G, have potent immunostimulatory activity. Therefore, these oligonucleotides can be administered to subjets to treat “immune system deficiencies” or in conjunction with a vaccine, as adjuvants, to boost the immune system in order to have a better response to the vaccine or administered to subjects to increase the responsiveness to tumors.

SUMMARY OF THE INVENTION

[0140] It has now been discovered that non-CpG oligonucleotides containing the following non-palindromic sequence motif:

X₁X₂X₃X₄X₅X₆X₇X₈,

[0141] wherein X₁, X₂ and X₇ are C,T,G or A; at least three of X₃, X_(4,) X₅, X₆ and X₈ are T; with the proviso that, in the motif, a C does not precede a G, are useful as inmmunostimulants in animals of the order Primate, including humans. According to a preferred embodiment, X₁ consist of a C or a T and X₇ consist of a G. More preferably X₃,X₄,X₅,X₆ X₇ X₈ of the immunostimulatory motif consist of TTTTGT. Even more advantageously X₁X₂X₃X₄X₅X₆X₇X₈ consist of CNTTTTGT or TNTTTTGT wherein N is C, T, G or A. Those of X₃-X₆ and X₈ that are not T can be any nucleotide (e.g., C, T, G, A) or can be absent so that the nucleotide preceding links directly with the nucleotide following the position of the omitted nucleotide (S). The oligonucleotides of this invention are useful as adjuvants in a vaccine formulation comprising one or more antigens. In embodiments of this aspect, the vaccine formulation can be liquid or lyophilized in dosage form. Many dosage forms are known in the art and can be applied herein. In embodiments of this aspect the oligonucleotides of this invention are present in the composition at a dose of from about 10 to 10,000 μg per dose. In these preparations the oligonucleotides of this invention may be combined with other immunostimulant compounds. Examples of well known immunostimulants are: α-interferon, β-interferon, γ-interferon, granulocyte macrophage colony stimulator factor (GM-CSF), interleukin 2 (IL2), interleukin 12 (IL12) and CpG oligonucleotide.

[0142] In preferred embodiments the antigenic component of the vaccine is one or more, natural or recombinant, antigens of viruses like: Human immunodeficiency viruses, such as HIV-1 and HIV-2, polio viruses, hepatitis A virus, human coxsackie viruses, rhinoviruses, echoviruses, equine encephalitis viruses, rubella viruses, dengue viruses, encephalitis viruses, yellow fever viruses, coronaviruses), vesicular stomatitis viruses, rabies viruses, ebola viruses, parainfluenza viruses, mumps virus, measles virus, respiratory syncytial virus, influenza viruses, Hantaan viruses, bunga viruses, hemorrhagic fever viruses, reoviruses, orbiviuises, rotaviruses, Hepatitis B virus, parvoviruses, papilloma viruses, polyoma viruses, adenoviruses), herpes simplex virus (HSV) 1 and 2, varicella zoster virus, cytomegalovirus (CMV), variola viruses, vaccinia viruses, pox viruses, African swine fever virus, the unclassified agent of delta hepatitis, the agents of non-A, non-B hepatitis; of infectious bacteria like: Helicobacter pylori, Borrelia burgdorferi, Legionella pneumophila, Mycobacterium tuberculosis, Mycobacterium bovis (BCG), Mycobacterium avium, Mycobacterium intracellulare, Staphylococcus aureus, Neisseria gonorrhoeae, Neisseria meningitidis, Listeria monocytogenes, Streptococcus pyogenes, Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catharralis, Klebsiella pneumoniae, Bacillus anthracis, Corynebacterium diphtheriae, Clostridium perfringers, Clostridium tetani, Enterobacter aerogenes, Klebsiella pneumoniae, Pasturella multocida, and Treponema pallidum; of infectious fungi like: Cryptococcus neoformans, Histoplasma capsulatum, Coccidioides immitis, Blastomyces dermatitidis, Candida albicans; of infectious protists like: Plasmodium falciparum, Trypanosoma cruzi, Leishmania donovani and Toxoplasma gondii. and; of human tumoral cells.

[0143] In embodiments of this aspect one or more of the oligonucleotides of this invention and the antigen are administered simultaneously locally (by oral, rectal, intranasal or transdermal route) or systemically (by intradermic or intramuscular injection). An aspect of this invention is a method of vaccination of a person. The person can be vaccinated prophylactically or therapeutically.

[0144] A prophylactic vaccine is designed to elicit protection from a disease caused by an infectious agent through the induction of specific immunity.

[0145] A therapeutic vaccine is designed to induce remission of an illness (i.e. a tumor and metastasis or illness associated with, an infectious agent like the human immunodeficiency virus).

[0146] The method of vaccination includes administering one or more of the oligonucleotides of this invention and one or more antigens—that is, the vaccine can be designed against one disease target or a combination of disease targets. Another aspect of this invention is a method of treatment of a person with a tumoral disease or an immunological disorder, with one or more of the oligonucleotides of this invention to stimulate his/her endogenous immune response. Examples of tumoral disease are: Chronic Myelogenous Leukemia, Precursor B-lymphoblastic lymphoma, B-cell chronic lymphocytic leukaemia, Lymphoplasmacytic lymphoma, Mantle cell lymphoma, Follicle center lymphoma, (follicular and diffuse), Marginal zone-B lymphoma, Extranodal lymphoma, Nodal marginal zone B-cell lymphoma, Splenic marginal zone B-cell lymphoma, Hairy cell leukaemia, Plasmocytoma, Diffuse large B-cell lymphoma, Burkitt's lymphoma, High grade B-cell lymphoma, Burkitt like, Melanoma, Kaposi's Sarcoma, Multiple Myeloma, Renal Cell Carcinoma, Bladder Cancer, Lung Cancer, Skin Cancer, Breast Cancer, Colon Cancer and Uterus Cancer. Examples of immunological disorders are: Allergy, Severe Combined Immunodeficiency, Chronic Granulomatous disease, and Acquired Immunodeficiency Disease.

[0147] In embodiments of this aspect, one or more of the oligonucleotide of this invention is/are present in a pharmaceutical formulation that can be liquid or lyophilized in dosage form. Many dosage forms are known in the art and can be applied herein. In embodiments of this aspect one or more of the oligonucleotides of this invention is/are present in the composition at a dose of from about 10 to 10,000 μg per dose. In these preparations one or more of the oligonucleotides of this invention may be combined with other immunostimulant compounds. Examples of well known immunostimulants are: α-interferon, β-interferon, γ-interferon, granulocyte macrophage colony stimulator factor (GM-CSF), interleukin 2 (IL2), interleukin 12 (IL12), CpG oligonucleotides and Mycobacterium bovis BCG cells. Also, one or more of the oligonucleotides of this invention may be combined with an antiinfective or anticancer drug, or a surgical procedure. In all these cases the oligonucleotides of this invention may be administered before, after or simultaneously with the alternative treatment.

[0148] Another aspect of this invention is a method of treatment of a person with a tumoral disease or an immunological disorder, contacting lymphocytes or plasmacytoid dendritic cells from the subject with one or more of the oligonucleotides of this invention “ex vivo” and readministering the activated cells to the subject. In embodiments of this aspect one or more of the oligonucleotides of this invention are present in the incubation media in a concentration of about 0.10 to 100 μg per ml.

BRIEF DESCRIPTION OF THE FIGURES

[0149]FIG. 1 is a graph plotting the proliferation index of human peripheral blood mononuclear leukocytes (PBMC) cultured with the phosphorothioate ODN IMT 023 (Seq. ID No 9), the phosphorothioate CpG ODN 2006:

[0150] 5′ TCGTCGTTTTGTCGTTTTGTCGTT 3′,

[0151] the phosphorothioate non-CpG ODN IMT 021 (SEQ ID NO: 1). Data represent the mean and standard deviation of five independent assays.

[0152]FIG. 2 shows the results from a flow cytometry study using human peripheral blood mononuclear leukocytes (PBMC) to determine the comparative effect of the phosphorothioate CpG ODN 2006:

[0153] 5′ TCGTCGTTTTGTCGTTTTGTCGTT 3′

[0154] and the phosphorothioate non-CpG ODN IMT 021 (SEQ ID NO: 1)on activation of the B cell population:

[0155] (2a) Representative flow cytometry diagrams comparing B cell activation by IMT 023, 2006 and IMT 021 (2b) Representative histograms of the flow cytometry diagrams showed in (a).

[0156]FIG. 3 shows the influence of the position of the immunostimulatory sequence motif (3a) X₁X₂X₃X₄X₅X₆X₇X₈ here disclosed on the immunostimulatory activity of non-CpG ODNs as measured by proliferation assay (3b) and IL-6 secretion assay (3c). Data represent the mean and standard deviation of three independent assays performed by quadruplicate each. FIG. 4 shows the induction of CD40 (4a), MHC I (4b) and MHC II (4c) on CD19+ cells (B cells) by non-CpG-ODNs bearing the immunostimulatory sequence motif X₁X₂X₃X₄X₅X₆X₇X₈ here disclosed. Human PMBC were cultured for 24 hr with indicated ODNs and then stained with fluorescent anti-CD19/anti-CD40 (4a) or, anti-CD19/anti-MHC I (4b) or, anti-MHC II (4c). Flow cytometric results are presented as histograms. Open histograms correspond to cells cultured in absence of ODN and shaded histograms to cells cultured in presence of ODN. ODN (S) means phosphorothioate ODN.

[0157]FIG. 5 shows the induction of CD86 (5a), CD40 (5b) and MHC I (5c) on purified B cells by non-CpG-ODNs bearing the immunostimulatory sequence motif X₁X₂X₃X₄X₅X₆X₇X₈ here disclosed. Human purified B cells were cultured for 24 hr with indicated ODNs and then stained with fluorescent anti-CD19/anti-CD86 (5a) or, anti-CD19/anti-CD40 (5b) or, anti-CD19/anti-MHC I (5c). Flow cytometric results are presented as histograms. Open histograms correspond to cells cultured in absence of ODN and shaded histograms to cells cultured in presence of ODN. ODN (S) means phosphorothioate ODN.

[0158]FIG. 6 shows induction of CD86 (6a), CD40 (6b) and MHC I (6c) in CD1 9+ cells (B cells) by phosphodiester non-CpG-ODNs bearing the immunostimulatory sequence motif X₁X₂X₃X₄X₅X₆X₇X₈ here disclosed. Human PMBC were cultured for 48 hr with indicated phosphodiester ODNs and then stained with fluorescent anti-CD19/anti-CD86 (6a) or, anti-CD19/anti-CD40 (6b) or, anti-CD19/anti-MHC I (6c). Flow cytometric results are presented as histograms. Open histograms correspond to cells cultured in absence of ODN and shaded histograms to cells cultured in presence of ODN. ODN (O) means phosphodiester ODN.

[0159]FIG. 7 shows stimulation of PMBC proliferation by non-CpG ODNs bearing the motif X₁X₂X₃X₄X₅X₆X₇X₈ here disclosed in non-human primates. Cebus apella (7a) or Macacca fascicularis PMBC (7b) were cultured for 72 hr with indicated ODNs (6 μg/ml). Data represent the mean and standard deviation of four replicates.

[0160]FIG. 8 shows the induction of CD86 (8a), CD40 (8b) and MHC I (8c) on CD 19+ (B cells) of a patient suffering B cell leukemia by non-CpG-ODNs bearing the motif X₁X₂X₃X₄X₅X₆X₇X₈ here disclosed. PMBC were cultured for 24 hr with indicated ODNs and then stained with fluorescent anti-CD19/anti-CD86 (8a) or, anti-CD19/anti-CD40 (8b) or, anti-CD19/anti-MHC I (8c). Flow cytometric results are presented as histograms. Open histograms correspond to cells cultured in absence of ODN and shaded histograms to cells cultured in presence of ODN. ODN (S) means phosphorothioate ODN.

[0161]FIG. 9 shows the induction of CD86 (9a), CD40 (9b) and MHC I (9c) on purified plasmacytoid dendritic cells by non-CpG-ODNs bearing the motif X₁X₂X₃X₄X₅X₆X₇X₈ here disclosed. More than 95 % pure plasmacytoid dendritic cells were cultured for 24 hr with indicated ODNs and then stained with fluorescent anti-CD19/anti-CD86 (9a) or, anti-CD19/anti-CD40 (9b) or, anti-CD19/anti-MHC I (9c). Flow cytometric results are presented as histograms. Open histograms correspond to cells cultured in absence of ODN and shaded histograms to cells cultured in presence of ODN. ODN (S) means phosphorothioate ODN.

DETAILED DESCRIPTION OF THE INVENTION

[0162] Definitions:

[0163] An “allergy” refers to acquired hypersensitivity to a substance (allergen). Examples of allergies are eczema, allergic rhinitis, asthma and urticaria.

[0164] An “immune system deficiency” refers to a disease in which the immune system is not functioning in normal capacity.

[0165] As used herein, the term “oligonucleotide” or “oligo” shall mean multiple nucleotides (i.e. molecules comprising a sugar (e.g. ribose or deoxyribose) linked to a phosphate group and to an exchangeable organic base, which is either a substituted pyrimidine (e.g. cytosine (C), thymine (T) or uracil (U)) or a substituted purine (e.g. adenine (A) or guanine (G)). The term “oligonucleotide” as used herein refers to both oligoribonucleotides (ORNs) and oligodeoxyribonucleotides (ODNs). The term “oligonucleotide” shall also include oligonucleosides (i.e. an oligonucleotide minus the phosphate) and any other organic base containing polymer. Oligonucleotides can be obtained from existing nucleic acid sources (e.g. genomic or cDNA), but are preferably synthetic (e.g. produced by oligonucleotide synthesis)

[0166] An “oligonucleotide” refers to multiple nucleotides linked by phosphodiester bonds.

[0167] An “immunostimulatory oligonucleotide” refers to an oligonucleotide which stimulates, (i.e. has a mitogenic effect on, or induces or increases cytokine expression by) a cell of the immune system (ie: a lymphocyte, a macrophage).

[0168] A “CpG” refers to an unmethylated cytosine-guanine dinucleotide.

[0169] A “CpG oligonucleotide” refers to an oligonucleotide which stimulates a cell of the immune system and its immunostimulatory activity critically depends of the presence of at least one CpG in its sequence.

[0170] A “non-CpG oligonucleotide” refers to an oligonucleotide which stimulates a cell of the immune system and its immunostimulatory activity does not critically depends of the presence of a CpG in its sequence.

[0171] A “subject” refers to an animal of the order Primate, including humans.

[0172] As used herein, the term “treating” refers to a process by which the symptoms of a disease, and more particularly infectious diseases or tumoral diseases or immunological disorders are ameliorated or completely eliminated.

[0173] As used herein, the term “preventing” refers to a process by which a disease, and more particularly infectious diseases or tumoral diseases or immunological disorders are obstructed or delayed.

[0174] In a preferred embodiment, the immunostimulatory oligonucleotides of the invention are advantageously modified into stabilized oligonucleotides. Such stabilized immunostimulatory oligonucleotide may be particularly useful to obtain a prolonged immunostimulation. As used herein, a “stabilized oligonucleotide” refers to an oligonucleotide that is relatively resistant to in vivo degradation (e.g. via an exo- or endo-nuclease). Preferred stabilized oligonucleotides of the present invention comprise a phosphate backbone modification. More particularly, the phosphate backbone modification is preferably a 5′ inter-nucleotide linkage modification, for instance, at the first two nucleotides of the 5′ end of the oligonucleotide of the invention. Furthermore, the phosphate backbone modification may be a 3′ inter-nucleotide linkage modification. In such a case, the modification may occur, for instance, at the last two nucleotides of the 3′ end of the oligonucleotide of the invention. Even more preferably, the immunostimulatory oligonucleotide of the invention may be stably modified so as to comprise a phosphorothioate-linked nucleotide (i.e. at least one of the phosphate oxygens is replaced by sulfur). In the most preferred embodiment, most if not all the nucleotides of the immunostimulatory oligonucleotides of the invention comprise a phosphorothioate-linked nucleotide.

[0175] Other stabilized oligonucleotides may alternatively include: nonionic DNA analogs, such as alkyl- and aryl-phosphonates (in which the charged phosphonate oxygen is replaced by an alkyl or aryl group), phosphodiester and alkylphosphotriesters, in which the charged oxygen moiety is alkylated. Oligonucleotides which contain a diol, such as tetraethyleneglycol or hexaethyleneglycol, at either or both termini have also been shown to be substantially resistant to nuclease degradation.

[0176] Description:

[0177] The present invention provides methods to augment the immune response of animals of the order Primate, including humans, adding to vaccines one or more of the oligonucleotides of this invention or performing a treatment based in the administration of one or more of the oligonucleotides of this invention to a person with a tumoral disease or an immunological disorder or contacting white blood cells obtained from a person with a tumoral disease or an immunological disorder with one or more of the oligonucleotides of this invention “ex vivo”, and readministering these activated white blood cells to the same person.

[0178] Vaccines compositions useful containing one or more of the oligonucleotides of this invention can present antigens directly (i.e., in the form of a defined protein or polysaccharide) or as a part of a complex biological entity (i.e. complete viruses; complete bacterial cells; bacterial membranes or artificial conjugates like polysaccharide-protein conjugates). These antigens can be combined in multiple vaccines.

[0179] A vaccine composition including at least one antigen is formulated to include one or more of the oligonucleotides of this invention.

[0180] For example the antigen can be Moraxella catharralis killed cells or subcellular fractions of these cells or Hepatitis B virus surface antigen natural or produced by means of the DNA recombinant technology.

[0181] One or more of the oligonucleotides of this invention may be formulated alone or together with one or more antigens in a pharmaceutical composition, which may also include carriers, thickeners, diluents, buffers, preservatives, surface active agents, anti-microbial agents, anti-inflammatory agents, anesthetics and the like. The formulation can be liquid or lyophilized. The pharmaceutical composition may be administered in a number of ways depending of whether local or systemic treatment is desired, and on the area to be treated. Administration may be done topically, orally, by inhalation or parenterally. Formulation for topical administration may include ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable. Formulations for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, capsules, tablets and the like. Thickeners, flavorings, diluents, emulsifiers and the like may be necessary or desirable. Formulations for parenteral administration include sterile aqueous solutions, which may also contain buffers, diluents and other additives. A vaccine containing one or more antigens and one or more of the oligonucleotides of this invention can be formulated and used for prophylactic or therapeutic purposes.

[0182] Common antigens used in viral prophylactic vaccines are from Hepatitis B virus, Hepatitis A virus and Influenza virus. Common antigens used in bacterial prophylactic vaccines are from Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catharralis, Klebsiella pneumoniae and Mycobacterium bovis (BCG). Common antigens used in therapeutic vaccines are from Papilloma virus, HIV virus and melanoma cells.

[0183] A further refinement of a vaccine formulation is to incorporate one or more of the oligonucleotides of this invention as adjuvant/s and the antigen/s into a delivery vehicle to provide for delayed release of the active compounds of the vaccine over time. This can be accomplished by various means known in the art. Examples of these means are encapsulation into Poly (lactide-coglicolide) micro particles (Kersten, G. F. A. and Gander, B. 1996. Biodegradable Micro Spheres as vehicles for antigens, in: S. H. E. Kaufmann, ed. Concepts in Vaccine Development. Walter de Gruyter. Berlin-N.Y.), liposomes (Gregoriadis, G. et al. 2000. Liposomes as Immunological Adjuvants and Vaccine Carriers, in: S. H. E. Kaufmann, ed. Concepts in Vaccine Development. Walter de Gruyter. Berlin-N.Y.) and poly (methyl methacrylate) nanoparticles (Kreuter, J. 2000. Poly (Methyl Methacrylate) nanoparticles as vaccine adjuvants, in: S. H. E. Kaufmann, ed. Concepts in Vaccine Development. Walter de Gruyter. Berlin-N.Y.).

[0184] Another refinement of the vaccine formulation is to conjugate the antigen/s and one or more of the oligonucleotides of this invention, by chemical means (Mier W, Eritja R, Mohammed A, Haberkorn U, Eisenhut M. 2000. Preparation and evaluation of tumor-targeting peptide-oligonucleotide conjugates. Bioconjug. Chem. 11:855).

[0185] Many vaccine formulations are known in the art and can be used by substituting one or more of the oligonucleotides of this invention for the adjuvant previously known or by simply adding one or more of the oligonucleotides of this invention to the original formulation.

[0186] Based on their immunostimulatory properties, one or more of the oligonucleotides of this invention can also be administered to a subject in vivo to treat a tumoral disease or an immune system disorder.

[0187] Examples of common tumoral diseases are: Chronic Myelogenous Leukemia, Melanoma, Kaposi's Sarcoma, Multiple Myeloma, Renal Cell Carcinoma, Bladder Cancer, Lung Cancer, Skin Cancer, Brest Cancer, Colon Cancer and Uterus Cancer. Examples of common immunological disorders are: Allergy, Severe Combined Immunodeficiency, Chronic Granulomatous disease, and Acquired Immunodeficiency Disease.

[0188] The pharmaceutical composition for these treatments may include one or more of the oligonucleotides of this invention together with carriers, thickeners, diluents, buffers, preservatives, surface active agents, anti-microbial agents, anti-inflammatory agents, anesthetics and the like. The formulation can be liquid or lyophilized.

[0189] The pharmaceutical composition may be administered in a number of ways depending of whether local or systemic treatment is desired, and on the area to be treated. Administration may be done topically, orally, by inhalation or parenterally. Formulation for topical administration may include ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable. Formulations for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, capsules, tablets and the like. Thickeners, flavorings, diluents, emulsifiers and the like may be necessary or desirable. Formulations for parenteral administration include sterile aqueous solutions, which may also contain buffers, diluents and other additives. Alternatively, one or more of the oligonucleotides of this invention can be contacted with immunocompetent cells (i.e. B cells or plasmacytoid dendritic cells) obtained from a subject having a tumoral disease or an immune system deficiency “ex vivo” and activated cells can then be reintroduced in the subject.

EXAMPLE 1

[0190] Materials and Methods

[0191] The following materials and methods were used generally throughout the examples.

[0192] 1) Oligonucleotides

[0193] Oligonucleotides having phosphorothioate internucleotide linkages were purchased, purified by high-pressure liquid chromatography (HPLC), from Operon Technologies (Alameda, Calif.) or Annovis (Aston, Pa.) or Oligos Etc (Bethel, Me.). Oligonucleotides were suspended in depyrogenated water and kept at −20° C. until used.

[0194] 2) Antibodies

[0195] Antibodies used in assays were purchased from Serotec (Raleigh, N.C.).

[0196] 3) Peripheric Blood Mononuclear Leukocytes (PBMC)

[0197] Blood was obtained by venipuncture from healthy donors using heparin as anticoagulant. PMBC were isolated by Ficoll-Hypaque (Sigma Diagnostics Inc., St. Louis, Mo.) density gradient centrifugation. Briefly, blood samples diluted 1:2 in RPMI-1640 medium (PAA laboratories GmbH, Linz, Austria) supplemented with 2.0 mM L-glutamine and 50.0 μg/ml gentamicin and 20 mM HEPES were centrifuged at 1000×g for 40 minutes at 20° C. PMBC were isolated, washed and suspended in medium supplemented with 10% fetal calf serum.

[0198] 4) Purification of Cells

[0199] B lymphocytes and plasmacytoid dendritic cells were purified from human PMBC by positive selection using the MACS magnetic cell separation systems (Miltenyi Biotec, Germany).

[0200] 5) Cell Proliferation Assays

[0201] Blood was obtained by venipuncture from healthy donors using heparin as anticoagulant. PMBC were isolated by Ficoll-Hypaque (Sigma Diagnostics Inc., St. Louis, Mo.) density gradient centrifugation. Briefly, blood samples diluted 1:2 in RPMI-1640 medium (PAA laboratories GmbH, Linz, Austria) supplemented with 2.0 mM L-glutamine and 50.0 μg/ml gentamicin and 20 mM HEPES were centrifuged at 1000×g for 40 minutes at 20° C. PMBC were isolated, washed and suspended in medium supplemented with 10% fetal calf serum.

[0202] 6) IL6 Assay

[0203] PBMC (3×10⁵/well) were cultured as described above with ODNs (6 μg/ml) for 24 hr. After this, supernatants were collected and IL6 levels measured by ELISA. Briefly, 96 well micro titer plates (NUNC, Denmark) were coated with anti-IL6 antibodies and blocked with RPMI 1640 media supplemented with 10% (v/v) heat inactivated FCS. IL6 was detected calorimetrically using biotin-labeled antibodies followed by peroxidase-conjugated strepto-avidin and then peroxidase-specific calorimetric substrate. Standard curves were generated using known amounts of recombinant IL6. The detection limit of these assays was 30 pg/ml. All assays were performed in duplicate.

[0204] 6) IgM Secretion Assay

[0205] PBMC (3×10⁵/well) were cultured as described above with ODNs (1.5 μg/ml) for 72 hr. After this, supernatants were collected and IgM assayed by ELISA. Briefly, 96 microtiter plates (NUNC, Denmark) were coated with anti-lgM antibodies and blocked with RPMI 1640 media. IgM was detected calorimetrically using peroxidase-labeled antibodies followed by peroxidase-specific calorimetric substrate. Standard curves were generated using known amounts of purified IgM. The detection limit of these assays was 50 ng/ml. All assays were performed in duplicate.

[0206] 6) Flow Cytometry

[0207] Staining of surface antigens was performed as described (J. Fló and E. Massouh. Age-related changes of native and memory CD4 rat lymphocyte subsets in mucosal and systemic lymphoid organs. Developmental and comparative Immunology 21: 443-453, 1997). Anti CD19 (Clone LT19), CD86 (Clone BU63), CD40 (clone LOB 7/6), CD4 (clone S 3.5), MHC class I (Clone W6/32) and MHC class II (Clone WR 18) antibodies were purchased from Serotec (Raleigh, N.C., USA).

[0208] Flow cytometric data of 10,000 cells/sample were acquired on a FACScan (Becton Dickinson Immunocytometry Systems, San Jose, Calif.). Data were analyzed using the computer program Win MDI, 2.8, Interface Flow Cytometry Application (Joseph Trotter Copyright 1993-1998).

[0209] 7) Immunization of Monkeys Against Hepatitis B Surface Antigen (HBsAg) and Evaluation of the Humoral Response

[0210] Twelve monkeys of the species Cebus Apella (2.5-3.5 Kg) were immunized with a pediatric dose of AgB (Pablo Cassara, Buenos Aires, Argentina) containing 10 μg of HBsAg adsobed to alumina (25 mg of Al³⁺/mg of HBsAg). This was administered alone (n=3, 1 female, 2 males) or combined with indicated phosphorothioate ODN (150 μg/dose) (n=3, 1 female, 2 males). All vaccines were administered intramuscular (i.m.) in the quadriceps muscle in a total volume of 1 ml. Monkeys were maintained in the animal facility of the CEMIC (Centro Medico de Investigaciones Clínicas), Buenos Aires, Argentina. Animals were monitored daily by specialists and weighed once per week. Plasma was recovered by intravenous (i.v.) puncture before and at various times after immunization and immediately assayed for antibodies using the commercial kit AUSAB (Abbot Laboratories, Illinois, USA). Titers are expressed in milliinternational units per ml.

EXAMPLE 2

[0211] Selection of Oligonucleotide Sequences

[0212] WO 96/02555 and U.S. Pat. No. 6,239,116 patents teach that to be immunostimulatory, oligonucleotides require sequences containing unmethylated CpG motifs (WO 96/02555, col. 13 lines 19-20 and U.S. Pat. No. 6,239,116, col. 6 lines 1-3). EP 0 468 520 teaches that to be immunostimulatory, oligonucleotides require a palindromic sequence of at least 6 nucleotides long to be satisfactory (EP 0 468 520, col. 11, lines 34-37). Therefore, several non-CpG oliqonucleotides, without palindromic sequences of at least 6 nucleotides long were probed using proliferation assays, cell differentiation assays, cytokine IL6 secretion assays and IgM secretion assays performed on human peripheral blood mononuclear leukocytes (PBMC). As a positive control, the CpG oligonucleotide 2006 of composition:

[0213] 5′ TCGTCGTTTTGTCGTTTTGTCGTT 3′

[0214] and phosphorothioate bonds described by Hartman and Krieg (Hartmann, G., Krieg, A. M. 2000. Mechanism and function of a newly identified CpG DNA motif in human primary B cells. J. Immunol. 164:944.) was used. As a background control the phosphorothioate oligonucleotide IMT 023 (SEQ ID No 9) or IMT 022 (SEQ ID No 8) with very low activity on human cells were used.

[0215] Also as a “presumably” negative control an oligonucleotide with the same composition of the oligonucleotide 2006 but in which all the CpG dinucleotides have been replaced by GpC dinucleotides:

[0216] 5′ TGCTGCTTTTGTGCTTTTGTGCTT 3′

[0217] was used. This oligonucleotide was named ODN IMT 021 (SEQ ID No 1).

[0218]FIG. 1 shows a proliferation assay performed with the above described oligonucleotides.

[0219] It was found, surprisingly, that the non CpG oligonucleotide IMT 021 was as active as the 2006 CpG oligonucleotide in proliferation assays (FIG. 1 and Table 1) if used at 1.5 mug/ml and approximately 40-60% active if used at 0.375 mug/ml. TABLE 1 Induction of peripheral white blood cell proliferation by Phosphorothioate CpG (2006) and non-CpG oligonucleotides (IMT 021) PROLIFERATION INDEX (ODN at 1.5 μg/ml) (ODN at 0.375 μg/ml) ODN (S) SEQUENCE (5′-3′) Avg. N SD Avg. N SD 2006 TCGTCGTTTTGTCGTTTTGTCGTT 17.95 4 2.39 13.83 14 1.55 IMT 021 TGCTGCTTTTGTGCTTTTGTGCTT 17.41 5 2.74 8.02 15 1.21

[0220] Immunostimulation was also evaluated by Flow Cytometry using the CD 19 general marker for human B cells and the CD 86 activation marker for human B cells.

[0221]FIG. 2 shows the activation of human B cells incubated with the non CpG ODN (S) IMT 021 as compared to the activation induced by incubation with the CpG ODN (S) 2006. As can be observed, both ODNs show similar activation pattern as compared with the ODN(S) IMT 023 background control.

[0222] IL6 secretion was also evaluated in supernatants of PBMC incubated with the CpG ODN (S) 2006 and the non CpG ODN (S) IMT 021 (Table 2). TABLE 2 Induction of human IL-6 secretion by phosphorothioate CpG and non-CpG oligonucleotides 2006 and IMT 021 IL-6 (pg/ml) ODN (S) expt. 1 expt. 2 expt. 3 expt. 4 cells alone 0 0 0 0 2006 568 159 597 374 IMT 021 348 384 836 596

[0223] Results of this assay also indicate that the non-CpG ODN (S) IMT 021 is an effective immunostimulant. Therefore, other non-CpG sequence variants of the 2006 oligonucleotide were investigated. Table 3 shows the results for six of these variants in which, the Cs or Gs of all the CpGs of this ODN were replaced by other nucleotides. As can be observed, the Gs of the CpGs in the ODN(S) 2006 are not necessary for B cell proliferation or IL6 secretion. However, modification of the Cs of the CpGs is detrimental if the replacement is for As or Gs but not if it is for Ts. These results clearly indicate that stimulation of the B cell proliferation and IL6 secretion by the ODN(S) 2006 is not at all associated with integrity of the CpG group. TABLE 3 Induction of peripheral white blood cell proliferation and IL6 secretion by non-CpG variants of the ODN(S) 2006 oligonucleotide PROLIFERATION INDEX IL-6 (pg/ml) (ODN at 0.375 μg/ml) (ODN at 6.0 μg/ml) ODN (S) SEQUENCE (5′-3′) Avg. N SD Avg. N SD 2006 TCGTCGTTTTGTCGTTTTGTCGTT 13.83 14 1.55 215.8 4 83.4 IMT 504 TCATCATTTTGTCATTTTGTCATT 13.08 2 3.80 285.2 2 39.5 IMT 505 TCCTCCTTTTGTCCTTTTGTCCTT 12.98 2 4.73 218.9 2 3.1 IMT 506 TCTTCTTTTTGTCTTTTTGTCTTT 11.66 4 2.77 228.9 4 161.0 IMT 501 TAGTAGTTTTGTAGTTTTGTAGTT 5.42 2 2.03 66.8 2 54.0 IMT 502 TGGTGGTTTTGTGGTTTTGTGGTT 7.16 2 3.24 89.7 2 91.4 IMT 503 TTGTTGTTTTGTTGTTTTGTTGTT 9.87 2 1.90 334.9 2 215.5

EXAMPLE 3

[0224] Effect of Structure Modification on the Immunostimulatory Activity of Non-CpG Oligonucleotides: Definition of the Active Motif.

[0225] In order to study the influence of the primary structure on the immunostimulatory activity of the non-CpG ODNs, several variants of the 2006 and IMT 021 oligonucleotides were synthesized. Table 4 shows the primary structure of some of the IMT 021 variants and the results of a proliferation and IL-6 assays performed in order to evaluate its immunostimulatory activity.

[0226] The ODN(S) IMT 021 contains T in positions 7,8,9,10,12,15,16,17,18,20,23 and 24. Replacement of these Ts with As (ODN IMT 022) or Cs (ODN IMT 023) results in a very significant loss of activity (about 76% and 75% respectively) in the proliferation assay and also in the IL-6 secretion assay (84% and 88% respectively). These results indicate that some or all the Ts in positions 7,8,9,10,12,15,16,17,18,20,23 and 24 are critical for the ODN IMT 021 immunostimulatory activity. TABLE 4 Induction of peripheral white blood cell proliferation and IL-6 secretion by Phosphorothioate non-CpG oligonucleotides derived from the inmunostimulatory IMT 021 oligonucleotide PROLIFERATION INDEX IL-6 (pg/ml) (ODN at 0.375 μg/ml) (ODN at 6.0 μg/ml) ODN (S) SEQUENCE (5′-3′) Avg. N SD Avg. N SD IMT 021 TGCTGCTTTTGTGCTTTTGTGCTT 8.02 15 1.21 181.3 4 49.9 IMT 022 TGCTGCAAAAGAGCAAAAGAGCAA 1.24 2 0.30 0.0 2 0.0 IMT 023 TGCTGCCCCCGCGCCCCCGCGCCC 1.07 4 0.12 0.0 3 0.0

[0227] The analysis of hundreds of ODNs (unshown) allowed definition of a core sequence (motif) responsible of the immunostimulatory activity as measured by B cell proliferation and IL6 secretion. This motif is the following:

X₁X₂X₃X₄X₅X₆X₇X₈,

[0228] wherein X₁ is C,T,G or A (preferably T or C);

[0229] wherein X₂ is C,T,G or A;

[0230] wherein X₇ is C,T,G or A (preferably G);

[0231] wherein at least three, and preferably all, of X₃, X₄, X₅, X₆ and X₈ are T.

[0232] Table 5 shows the effect of changes in each of the nucleotides of the two non-CpG motifs present in the ODN IMT 504 (motif: CATTTTGT). Replacement of the C in position 1 of the motif by A (ODN IMT 531) or G (ODN IMT 533) resulted in a loss of about 50% in the activity. However, replacement of this C by T (ODN IMT 532) does not change the activity. Thus, in order to obtain maximal activity the first position of the motif should be occupied by a pyrimidine nucleotide (C or T). In position 2, A (ODN IMT 504) or T (ODN IMT 535) or C (ODN IMT 534) are equivalent options.

[0233] In order to study the influence of a G nucleotide in position 2 of the motif without introduction of a CpG dinucleotide, ODNs with a T in the first position of the motif were synthesized (Table 6). As can be observed, any nucleotide in the second position of the immunostimulatory motif is equivalent.

[0234] Replacement of the G in position 7 of the immunostimulatory motif by A (ODN IMT 541), T (ODN IMT 542) or C (ODN IMT 543) is detrimental (Table 5). Thus, in order to obtain maximal activity position 7 should be preferably G.

[0235] Regarding to the positions of the immunostimulatory motif occupied by Ts, the most sensitive (as measured by a change for an A) are 4 (ODN IMT 538), 5 (ODN ITM 539) and 8 (ODN IMT 544) and less sensitive are 3 (ODN IMT 537) and 6 (ODN IMT 540). Replacement of two or more of the Ts within the motif results in more than 70% loss of activity (ODNs IMT 545, IMT 546, IMT 547, IMT 548, IMT 549, IMT 550, IMT 551 and IMT 552). Therefore, in order to obtain a significant immunostimulatory activity three or more of positions 3,4,5,6 and 8 should be occupied by T. TABLE 5 Induction of peripheral white blood cell proliferation and IL-6 secretion by phosphorothioate non-CpG oligonucleotides of this invention derived from ODN IMT 504 PROLIFERATION INDEX IL-6 (pg/ml) (ODN at 0.375 μg/ml) (ODN at 6.0 μg/ml) ODN (S) SEQUENCE (5′-3′) Avg. N SD Avg. N SD IMT 022 TGCTGCAAAAGAGCAAAAGAGCAA 1.34 24 0.52 42.7 6 29.7 IMT 504 TCATCATTTTGTCATTTTGTCATT 13.85 16 4.36 171.6 6 39.8 IMT 531 TCATAATTTTGTAATTTTGTCATT 7.59 12 2.71 137.4 6 124.4 IMT 532 TCATTATTTTGTTATTTTGTCATT 13.80 12 3.41 124.2 6 78.4 IMT 533 TCATGATTTTGTGATTTTGTCATT 6.20 12 2.71 118.3 6 76.0 IMT 534 TCATCCTTTTGTCCTTTTGTCATT 11.67 12 4.49 173.7 6 31.4 IMT 535 TCATCTTTTTGTCTTTTTGTCATT 12.49 12 2.51 160.6 6 39.0 IMT 537 TCATCAATTTGTCAATTTGTCATT 10.17 12 4.00 183.5 6 63.6 IMT 538 TCATCATATTGTCATATTGTCATT 7.12 12 2.95 133.2 6 86.7 IMT 539 TCATCATTATGTCATTATGTCATT 9.80 12 4.22 171.7 6 53.4 IMT 540 TCATCATTTAGTCATTTAGTCATT 11.94 12 2.55 163.1 6 43.0 IMT 541 TCATCATTTTATCATTTTATCATT 9.30 12 2.20 177.2 6 40.4 IMT 542 TCATCATTTTTTCATTTTTTCATT 9.78 12 2.60 151.1 6 40.2 IMT 543 TCATCATTTTCTCATTTTCTCATT 4.75 12 2.25 137.9 6 77.6 IMT 544 TCATCATTTTGACATTTTGACATT 7.16 12 2.11 124.4 6 42.7 IMT 545 TCATCATTTAGACATTTAGACATT 4.19 12 1.81 129.4 6 53.8 IMT 546 TCATCATTATGACATTATGACATT 2.90 12 1.16 105.0 6 67.2 IMT 547 TCATCATATTGACATATTGACATT 3.34 12 1.16 110.3 6 43.5 IMT 548 TCATCATTAAGACATTAAGACATT 3.40 12 1.53 91.5 6 33.1 IMT 549 TCATCATATAGACATATAGACATT 3.51 12 1.03 121.3 6 41.3 IMT 550 TCATCATAATGACATAATGACATT 1.91 12 0.71 79.3 6 30.8 IMT 551 TCATCATAAAGACATAAAGACATT 2.17 12 0.72 60.7 6 26.4 IMT 552 TCATCAAAAAGACAAAAAGACATT 1.37 12 0.83 21.6 6 13.5

[0236] TABLE 6 Induction of peripheric white blood cell proliferation and IL-6 secretion by Phosphorothioate non-CpG oligonucleotides with T in the first position of the immunostimulatory motif PROLIFERATION INDEX IL-6 (pg/ml) (ODN at 0.375 μg/ml) (ODN at 6.0 μg/ml) ODN (S) SEQUENCE (5′-3′) Avg. N SD Avg. N SD IMT 532 TCATTATTTTGTTATTTTGTCATT 10.10 4 1.61 221.7 4 35.3 IMT 197 TCATTTTTTTGTTTTTTTGTCATT 10.84 4 1.06 386.1 4 123.3 IMT 198 TCATTGTTTTGTTGTTTTGTCATT 10.00 4 1.75 235.3 4 27.1 IMT 199 TCATTCTTTTGTTCTTTTGTCATT 12.36 3 1.71 235.0 4 6.0

[0237] To investigate the effect of changes in the position of the motif within the ODN chain, the non-CpG motif CATTTTGT present in ODN IMT504 was introduced into different locations in a 24 nucleotides long poly T chain (FIG. 3). As can be seen, the poly T ODN (S) by itself has a significant mitogenic activity. On the other hand, introduction of only one CATTTTGT motif results in an increment of 1.2 to 1.8 times as measured by proliferation assays, or 2.4 to 3.5 times as measured by IL-6 secretion assays, in the immunostimulatory activity of the polyT chain depending on where the motif is located. A distance of at least two nucleotides from the 5′ end or four from the 3′ end seems to be necessary in order to reach maximal activity (ODNs IMT174 to IMT 179). Introduction of two motifs in optimal positions (ODN IMT182) results in an increment of 1.9 times as measured by proliferation assays, or 2.9 times as measured by IL-6 secretion assays, in the immunostimulatory activity of the polyT chain. This indicate that contribution of the second motif is negligible. On the other hand, the activity of the most effective ODNs like ODN IMT504 is more than 3 times larger than the activity of the poly T as measured by proliferation assays a fact that suggest that there is also a significant influence of the composition of at least some of the nucleotides surrounding the motif of this invention, in the overall activity of the ODN.

EXAMPLE 4

[0238] Effect of Structure Modification on the Immunostimulatory Activity of Non-CpG Oligonucleotides of this Invention: Influence of the Nucleotide Composition Outside of the Active Motif.

[0239] Results shown in FIG. 3 indicate that composition of the oligonucleotide outside the non-CpG core motif is important in order to reach optimal immunostimulatory activity. Therefore, a number of oligonucleotides were synthesized with changes in the composition of the nucleotides surrounding the motifs. Table 7 shows the effect of changes in the composition of the first four nucleotides of the 5′ end and of the last four nucleotides the 3′ end in the immunostimulatory activity of ODN IMT 504. As can be observed, the best choices are: C or G in position −1 respect to the two motifs, C, T or G in position −2, any nucleotide in positions −3 and −4, A or T in position +1, G in position +2, any nucleotide in positions +3 and G is the best choice in position +4 .

[0240] Of course, other nucleotide combinations not represented in this table may have equal or even better effect on the activity of the non CpG immunostimulatory oligonucleotides. One of ordinary skill in the art can empirically determine other effective combinations. TABLE 7 Induction of peripheric white blood cell proliferation by non-CpG ODN(S) IMT 504 with variations in the composition outside the two immunostimulatory motifs PROLIFERATION INDEX IL-6 (pg/ml) (ODN at 0.375 μg/ml) (ODN at 6.0 μg/ml) ODN (S) SEQUENCE (5′-3′) Avg. N SD Avg. N SD IMT 552 TGCTGCAAAAGAGCAAAAGAGCAA 1.9 12 0.7 <39.9 4 — IMT 504 TCATCATTTTGTCATTTTGTCATT 11.0 8 0.9 171 2 14 IMT 559 ACATCATTTTGTCATTTTGTCATT 13.4 4 1.0 128 3 3 IMT 560 CCATCATTTTGTCATTTTGTCATT 12.1 4 0.9 145 4 32 IMT 561 GCATCATTTTGTCATTTTGTCATT 9.5 4 1.1 209 4 74 IMT 562 TAATCATTTTGTCATTTTGTCATT 12.4 4 1.5 171 4 24 IMT 563 TTATCATTTTGTCATTTTGTCATT 11.1 3 0.7 172 4 63 IMT 564 TGATCATTTTGTCATTTTGTCATT 12.8 4 0.9 118 4 38 IMT 565 TCCTCATTTTGTCATTTTGTCATT 14.1 4 0.5 135 4 25 IMT 566 TCTTCATTTTGTCATTTTGTCATT 13.9 4 2.2 157 4 28 IMT 567 TCGTCATTTTGTCATTTTGTCATT 12.9 4 0.7 259 4 25 IMT 568 TCAACATTTTGTCATTTTGTCATT 10.3 4 1.1 153 4 35 IMT 569 TCACCATTTTGTCATTTTGTCATT 15.0 4 1.2 199 3 12 IMT 570 TCAGCATTTTGTCATTTTGTCATT 12.5 4 0.4 181 3 2 IMT 571 TCATCATTTTGTCATTTTGTAATT 14.2 4 0.7 163 4 26 IMT 572 TCATCATTTTGTCATTTTGTTATT 13.2 4 1.4 182 3 67 IMT 573 TCATCATTTTGTCATTTTGTGATT 8.7 4 0.7 177 4 29 IMT 574 TCATCATTTTGTCATTTTGTCCTT 8.1 4 0.7 179 3 58 IMT 575 TCATCATTTTGTCATTTTGTCTTT 10.8 4 0.8 150 3 47 IMT 576 TCATCATTTTGTCATTTTGTCGTT 12.6 4 1.1 202 4 55 IMT 577 TCATCATTTTGTCATTTTGTCAAT 10.0 4 1.4 243 3 8 IMT 578 TCATCATTTTGTCATTTTGTCACT 10.9 4 0.9 213 2 9 IMT 579 TCATCATTTTGTCATTTTGTCAGT 10.7 4 1.7 182 4 18 IMT 580 TCATCATTTTGTCATTTTGTCATA 11.7 4 1.4 194 4 36 IMT 581 TCATCATTTTGTCATTTTGTCATC 10.7 4 1.0 173 4 18 IMT 582 TCATCATTTTGTCATTTTGTCATG 12.1 4 0.8 242 3 231

EXAMPLE 5

[0241] Effect of Structure Modification on the Immunostimulatory Activity of Non-CpG Oligonucleotides of this Invention: Influence of the Size of the Oligonucleotide

[0242] Table 8 shows that ODNs with one immunostimulatory motif are active if the chain is 16 or more nucleotides long. Activity is maximal if the ODN is 20 or more nucleotides long. TABLE 8 Effect of the phosphorothioate non-CpG oligonucleotides size on B cells proliferation and IL6 secretion PROLIFERATION INDEX IL-6 (pg/ml) (ODN at 0.375 μg/ml) (ODN at 6.0 μg/ml) ODN (S) SEQUENCE (5′-3′) Avg. N SD Avg. N SD IMT 187 TTTTCATTTTGT 0.56 8 0.20 <50 4 — IMT 188 TTTTCATTTTGTTTTT 2.76 8 1.73 147 4 40 IMT 189 TTTTCATTTTGTTTTTTTTT 8.21 8 3.19 227 4 21 IMT 175 TTTTCATTTTGTTTTTTTTTTTTT 8.92 8 1.80 220 4 18 IMT 179 TTTTTTTTTTTTCATTTTGTTTTT 6.06 8 2.00 224 4 82 IMT 191 TTTTCATTTTGTTTTTTTTTTTTTTTTT 6.64 8 2.37 205 4 15

EXAMPLE 6

[0243] Induction of Peripheric White Blood Cell IgM Secretion by Phosphorothioate Non-CpG Oligonucleotides of this Invention

[0244] Induction of IgM secretion in peripheral white blood cells is another important marker of immunostimulatory activity of oligonucleotides. Table 9 shows the stimulation of IgM secretion by several of the phosphorothioate non-CpG oligonucleotides described above. As can be observed, the most active non-CpG ODN(S)s in induction of proliferation and IL6 secretion are also the best in induction of IgM secretion. TABLE 9 Induction of peripheral white blood cell IgM secretion by phosphorothioate non-CpG oligonucleotides of this invention IgM SECRETION (ng/ml) (ODN at 1.50 μg/ml) ODN (S) SEQUENCE (5′-3′) Avg. N SD cells alone 76 9 50 2006 TCGTCGTTTTGTCGTTTTGTCGTT 778 47 204 IMT 021 TGCTGCTTTTGTGCTTTTGTGCTT 850 25 264 IMT 501 TAGTAGTTTTGTAGTTTTGTAGTT 585 25 179 IMT 502 TGGTGGTTTTGTGGTTTTGTGGTT 555 19 277 IMT 503 TTGTTGTTTTGTTGTTTTGTTGTT 640 19 220 IMT 504 TCATCATTTTGTCATTTTGTCATT 912 24 244 IMT 505 TCCTCCTTTTGTCCTTTTGTCCTT 664 23 336 IMT 506 TCTTCTTTTTGTCTTTTTGTCTTT 751 43 237 IMT 509 AAAAAACTAAAAAAAACTAAAAAA 195 17 77

EXAMPLE 7

[0245] Stimulation of the Expression of CD40, MHC I and MHC II in B Lymphocytes by Phosphorothioate Non-CpG Oligonucleotides of this Invention

[0246] As previously shown (FIG. 2), the non CpG ODN IMT 021 is able to stimulate the expression of CD86 on CD19+ cells (B lymphocytes). In order to extent this observation to other important cell surface markers, human PMBC were incubated with ODN IMT 504, ODN 2006 as a positive control and ODN IMT 022 as a negative control (FIG. 4). As can be observed, ODN IMT 504 is as active as the CpG ODN 2006 for stimulation of the expression of CD40, MHC I and MHC II on B lymphocytes.

EXAMPLE 8

[0247] Stimulation of Purified B Lymphocytes by Non-CpG Oligonucleotides of this Invention

[0248] Human CD19⁺ (B) cells were purified to more than 95% purity. Table 10 and FIG. 5 shows that the immunostimulatory activity on this purified cells is comparable to the one observed using human PMBC. These results indicate that stimulation by the non-CpG oligonucleotides of this invention on human cells is direct. TABLE 10 Induction of proliferation, IL6 and IgM secretion on purified B cells by phosphorothioate non-CpG oligonucleotides of this invention Proliferation Index IL-6 (pg/ml) IgM (ng/ml) (ODN at 0.375 μg/ml) (ODN at 6.0 μg/ml) (ODN at 1.5 μg/ml) ODN (S) SEQUENCE (5′-3′) Ave. N SD Ave. N SD Ave. N SD IMT 022 TGCTGCAAAAGAGCAAAAGAGCAA 1.28 16 0.80 1019 5 665 469 7 182 IMT 021 TGCTGCTTTTGTGCTTTTGTGCTT 24.48 16 5.16 9588 5 729 946 9 386 IMT 504 TCATCATTTTGTCATTTTGTCATT 47.95 16 6.41 11002 5 884 1274 9 252 IMT 506 TCTTCTTTTTGTCTTTTTGTCTTT 25.58 16 7.84 10933 3 1628 1083 10 430 2006 TCGTCGTTTTGTCGTTTTGTCGTT 60.82 24 9.79 7631 6 997 1292 12 245

EXAMPLE 9

[0249] Immunostimulation by Phosphodiester Non-CpG Oligonucleotides of this Invention

[0250]FIG. 6 and Table 11 shows the effect of phosphodiester non-CpG oligonucleotides of this invention on human PMBC. Since phosphodiester oligonucleotides are very sensitive to nucleases they were added to the culture three times (0, 4, and 16 hs) to a final concentration of 30 μg/ml. A very potent phosphodiester CpG ODN (ODN 2080) was used as positive control in cytometric assays (Hartmann G, Weeratna R, Ballas Z K, Payette P, Suparto, I, Rasmussen W L, Wadschmidt M, Sajuthi D, Purcells R H, Davis H L, Krieg A M. Delineation of a CpG phosphorothioate oligodeoxynucleotide for activating primate immune responses in vitro and in vivo. J. Immunol.164, 1617-1624, (2000)). As can be observed, under these conditions phosphodiester ODNs bearing non CpG motifs of this invention have immunostimulatory activity. TABLE 11 Immune-stimulation by phosphodiester non-CpG oligonucleotides of this invention IL-6 Secretion (ng/ml) (ODN at 6.0 μg/ml) ODN (S) SEQUENCE (5′-3′) Avg. N SD IMT 022 TGCTGCAAAAGAGCAAAAGAGCAA 23 8 10 IMT 053 TTTTTTTTTTTTTTTTTTTTTTTT 24 4 24 IMT 504 TCATCATTTTGTCATTTTGTCATT 207 6 46 IMT 506 TCTTCTTTTTGTCTTTTTGTCTTT 403 3 220 2006 TCGTCGTTTTGTCGTTTTGTCGTT 228 4 40

EXAMPLE 10

[0251] Induction of Cell Proliferation in Peripheral White Blood Cells of Monkeys of the Species Cebus apella and Macaca fascicularis by Non-CpG ODN(S)s of this Invention

[0252] Non-CpG ODN(S)s of this invention are not very effective immunostimulants in mouse, pig and sheep. However, they are effective in monkeys. For example, FIG. 7 shows the immunostimulatory activity of non-CpG ODN(S)s on peripheral white blood cells of monkeys of the species Cebus apella and Macaca fascicularis. According to these results the most effective non-CpG ODNs in primates are those bearing the CATTTTGT motif. Therefore, monkeys can be used as animal models for research on clinical applications of these non-CpG ODN(S)s.

EXAMPLE 11

[0253] Vaccination of Subjects

[0254] Vaccine formulations containing the non-CpG ODNs adjuvant of this invention can be used to vaccinate subjects against a variety of bacterial and viral disease agents and against tumoral cells. Table 12 shows the effect of inoculation of monkeys of the species Cebus apella with a vaccine formulation that includes recombinant Hepatitis B surface antigen (rHBsAg) and alumina in presence or absence of ODN IMT 504 or ODN IMT 021 as adjuvant. TABLE 12 Anti-HBs responses in Cebus apella immunized against HBsAg with IMT ODNs Post - prime Post - boost ODN (S) Pre - prime 14 days 28 days 14 days None 0 0.4 ± 0.1 14 ± 20 190 ± 52  IMT 021 0 23 ± 32 231 ± 287 902 ± 169 IMT 504 0 10 ± 14 113 ± 114 659 ± 296 2006 0 22 ± 24 67 ± 57 705 ± 315

[0255] As can be observed there is a dramatic increment in the title of anti-HBsAg in animals vaccinated with HBsAg plus IMT ODN(S) 504 or 21 as compared with those vaccinated with HBsAg alone. CpG ODN 2006 have a performance as adjuvant similar to the non-CpG ODNs of this invention.

[0256] In particular, a human can be vaccinated against hepatitis B by administration of a vaccine formulation that includes recombinant Hepatitis B surface antigen (rHBsAg) and alumina and one or more of the oligonucleotides of this invention as adjuvants. The amount of rHBsAg in each dose, and the administration schedule, can vary as appropriate for the age of the human. For example, for humans from about birth to about 12 years old, a three dose schedule of from about 2.5 μg to about 5 μg of rHBsAg can be administered at 0, 1-3 months afterward and 4-18 months afterward, preferably at 0, 2 and 6 months. One or more of the oligonucleotides of this invention can be present in the formulation from about 10 μg to about 1,000 μg per dose.

[0257] For humans from about 12 to about 60 years old, a three dose schedule of from about 5 μg to about 40 μg of rHBsAg can be administered at 0, 1-3 months afterward and 4-18 months afterward, preferably at 0, 2 and 6 months. One or more of the oligonucleotides of this invention can be present in the formulation from about 10 μg to about 1,000 μg per dose.

EXAMPLE 12

[0258] Stimulation of the Expression of Costimulatory Molecules in Malignant B-Lymphocytes by Phosphorothioate Non-CpG Oligonucleotides

[0259] The stimulation of malignant B lymphocytes recovered from blood of patients suffering chronic lymphocytic leukemia (CLL) by phosphorothioate non-CpG oligonucleotides of this invention was examined by flow cytometric (FACS) analysis. The results of a typical FACS analysis are shown in FIG. 8.

[0260] As can be seen the phosphorothioate non-CpG oligonucleotides IMT 021 and IMT 504 of this invention are able to stimulate expression of CD86, CD40 and MHC class I surface costimulatory molecules on malignant B lymphocytes as well as the CpG ODN 2006.

EXAMPLE 13

[0261] Stimulation of the Expression of Costimulatory Molecules on Plasmacytoid Dendritic Cells by Phosphorothioate Non-CpG Oligonucleotides of this Invention

[0262] The stimulation of plasmacytoid dendritic cells recovered from blood of normal donors by phosphorothioate non-CpG oligonucleotides of this invention was examined by flow cytometric (FACS) analysis. The results of a typical FACS analysis are shown in FIG. 9. As can be seen the phosphorothioate non-CpG oligonucleotides IMT 021 and IMT 504 of this invention are able to stimulate expression of CD86, CD40 and MHC class I surface molecules on plasmacytoid dendritic cells as well as the CpG ODN 2006.

EXAMPLE 14

[0263] Treatment of Subjects with Tumoral Disease

[0264] Pharmaceutical formulations containing one or more of the oligonucleotides immunostimulatory of this invention, can be used to treat subjects against a variety of tumoral diseases. In particular, a human with a Melanoma can be treated by administration of a pharmaceutical formulation containing the oligonucleotide of this invention as the active component. The amount of oligonucleotide in each dose, and the administration schedule, can vary appropriate for the corporal mass of the subject and stage in tumor progression. For example, for a human of about 70 Kg. having an advance, unresectable metastatic melanoma, a dose of about 1 mg of the oligonucleotide of this invention can be administered 3 times per week during about 10 weeks.

1 74 1 24 DNA Artificial Sequence PCR primer 1 tgctgctttt gtgcttttgt gctt 24 2 24 DNA Artificial Sequence PCR primer 2 tcatcatttt gtcattttgt catt 24 3 24 DNA Artificial Sequence PCR primer 3 tcctcctttt gtccttttgt cctt 24 4 24 DNA Artificial Sequence PCR primer 4 tcttcttttt gtctttttgt cttt 24 5 24 DNA Artificial Sequence PCR primer 5 tagtagtttt gtagttttgt agtt 24 6 24 DNA Artificial Sequence PCR primer 6 tggtggtttt gtggttttgt ggtt 24 7 24 DNA Artificial Sequence PCR primer 7 ttgttgtttt gttgttttgt tgtt 24 8 24 DNA Artificial Sequence PCR primer 8 tgctgcaaaa gagcaaaaga gcaa 24 9 24 DNA Artificial Sequence PCR primer 9 tgctgccccc gcgcccccgc gccc 24 10 24 DNA Artificial Sequence PCR primer 10 tcattttttt gtttttttgt catt 24 11 24 DNA Artificial Sequence PCR primer 11 tcattgtttt gttgttttgt catt 24 12 24 DNA Artificial Sequence PCR primer 12 tcattctttt gttcttttgt catt 24 13 24 DNA Artificial Sequence PCR primer 13 aaaaaactaa aaaaaactaa aaaa 24 14 24 DNA Artificial Sequence PCR primer 14 tcataatttt gtaattttgt catt 24 15 24 DNA Artificial Sequence PCR primer 15 tcattatttt gttattttgt catt 24 16 24 DNA Artificial Sequence PCR primer 16 tcatgatttt gtgattttgt catt 24 17 24 DNA Artificial Sequence PCR primer 17 tcatcctttt gtccttttgt catt 24 18 24 DNA Artificial Sequence PCR primer 18 tcatcttttt gtctttttgt catt 24 19 24 DNA Artificial Sequence PCR primer 19 tttttttttt tttttttttt tttt 24 20 24 DNA Artificial Sequence PCR primer 20 cattttgttt tttttttttt tttt 24 21 24 DNA Artificial Sequence PCR primer 21 ttcattttgt tttttttttt tttt 24 22 24 DNA Artificial Sequence PCR primer 22 ttttcatttt gttttttttt tttt 24 23 24 DNA Artificial Sequence PCR primer 23 ttttttcatt ttgttttttt tttt 24 24 24 DNA Artificial Sequence PCR primer 24 ttttttttca ttttgttttt tttt 24 25 24 DNA Artificial Sequence PCR primer 25 tttttttttt cattttgttt tttt 24 26 24 DNA Artificial Sequence PCR primer 26 tttttttttt ttcattttgt tttt 24 27 24 DNA Artificial Sequence PCR primer 27 tttttttttt ttttcatttt gttt 24 28 24 DNA Artificial Sequence PCR primer 28 tttttttttt ttttttcatt ttgt 24 29 24 DNA Artificial Sequence PCR primer 29 ttttcatttt gtcattttgt tttt 24 30 24 DNA Artificial Sequence PCR primer 30 tcatcaattt gtcaatttgt catt 24 31 24 DNA Artificial Sequence PCR primer 31 tcatcatatt gtcatattgt catt 24 32 24 DNA Artificial Sequence PCR primer 32 tcatcattat gtcattatgt catt 24 33 24 DNA Artificial Sequence PCR primer 33 tcatcattta gtcatttagt catt 24 34 24 DNA Artificial Sequence PCR primer 34 tcatcatttt atcattttat catt 24 35 24 DNA Artificial Sequence PCR primer 35 tcatcatttt ttcatttttt catt 24 36 24 DNA Artificial Sequence PCR primer 36 tcatcatttt ctcattttct catt 24 37 24 DNA Artificial Sequence PCR primer 37 tcatcatttt gacattttga catt 24 38 24 DNA Artificial Sequence PCR primer 38 tcatcattta gacatttaga catt 24 39 24 DNA Artificial Sequence PCR primer 39 tcatcattat gacattatga catt 24 40 24 DNA Artificial Sequence PCR primer 40 tcatcatatt gacatattga catt 24 41 24 DNA Artificial Sequence PCR primer 41 tcatcattaa gacattaaga catt 24 42 24 DNA Artificial Sequence PCR primer 42 tcatcatata gacatataga catt 24 43 24 DNA Artificial Sequence PCR primer 43 tcatcataat gacataatga catt 24 44 24 DNA Artificial Sequence PCR primer 44 tcatcataaa gacataaaga catt 24 45 24 DNA Artificial Sequence PCR primer 45 tcatcaaaaa gacaaaaaga catt 24 46 24 DNA Artificial Sequence PCR primer 46 acatcatttt gtcattttgt catt 24 47 24 DNA Artificial Sequence PCR primer 47 ccatcatttt gtcattttgt catt 24 48 24 DNA Artificial Sequence PCR primer 48 gcatcatttt gtcattttgt catt 24 49 24 DNA Artificial Sequence PCR primer 49 taatcatttt gtcattttgt catt 24 50 24 DNA Artificial Sequence PCR primer 50 ttatcatttt gtcattttgt catt 24 51 24 DNA Artificial Sequence PCR primer 51 tgatcatttt gtcattttgt catt 24 52 24 DNA Artificial Sequence PCR primer 52 tcctcatttt gtcattttgt catt 24 53 24 DNA Artificial Sequence PCR primer 53 tcttcatttt gtcattttgt catt 24 54 24 DNA Artificial Sequence PCR primer 54 tcgtcatttt gtcattttgt catt 24 55 24 DNA Artificial Sequence PCR primer 55 tcaacatttt gtcattttgt catt 24 56 24 DNA Artificial Sequence PCR primer 56 tcaccatttt gtcattttgt catt 24 57 24 DNA Artificial Sequence PCR primer 57 tcagcatttt gtcattttgt catt 24 58 24 DNA Artificial Sequence PCR primer 58 tcatcatttt gtcattttgt aatt 24 59 24 DNA Artificial Sequence PCR primer 59 tcatcatttt gtcattttgt tatt 24 60 24 DNA Artificial Sequence PCR primer 60 tcatcatttt gtcattttgt gatt 24 61 24 DNA Artificial Sequence PCR primer 61 tcatcatttt gtcattttgt cctt 24 62 24 DNA Artificial Sequence PCR primer 62 tcatcatttt gtcattttgt cttt 24 63 24 DNA Artificial Sequence PCR primer 63 tcatcatttt gtcattttgt cgtt 24 64 24 DNA Artificial Sequence PCR primer 64 tcatcatttt gtcattttgt caat 24 65 24 DNA Artificial Sequence PCR primer 65 tcatcatttt gtcattttgt cact 24 66 24 DNA Artificial Sequence PCR primer 66 tcatcatttt gtcattttgt cagt 24 67 24 DNA Artificial Sequence PCR primer 67 tcatcatttt gtcattttgt cata 24 68 24 DNA Artificial Sequence PCR primer 68 tcatcatttt gtcattttgt catc 24 69 24 DNA Artificial Sequence PCR primer 69 tcatcatttt gtcattttgt catg 24 70 12 DNA Artificial Sequence PCR primer 70 ttttcatttt gt 12 71 16 DNA Artificial Sequence PCR primer 71 ttttcatttt gttttt 16 72 20 DNA Artificial Sequence PCR primer 72 ttttcatttt gttttttttt 20 73 24 DNA Artificial Sequence PCR primer 73 tttttttttt ttcattttgt tttt 24 74 28 DNA Artificial Sequence PCR primer 74 ttttcatttt gttttttttt tttttttt 28 

1. A immunostimulatory oligonucleotide having about 14 to 100 nucleotides, comprising a non palindromic nucleic acid sequence motif having the following formula: X₁X₂X₃X₄X₅X₆X₇X₈, wherein X₁ is C,T,G or A; X₂ is C,T,G or A; X₇ is C,T,G or A; and at least three of X₃, X_(4,) X₅, X₆ and X₈ are T; with the proviso that, in the motif, a C does not precede a G.
 2. The immunostimulatory oligonucleotide of claim 1, wherein X₁ consists of a C.
 3. The immunostimulatory oligonucleotide of claim 1, wherein X₁ is C,T,G or A; X₇ is C,T,G or A; and all, of X₃, X₄, X₅, X₆ and X₈ are T.
 4. The immunostimulatory oligonucleotide of claim 1, wherein X₃X₄X₅X₆X₇X₈ consists of TTTTGT or TTTTCT.
 5. The immunostimulatory oligonucleotide of claim 1 wherein X₁ is T or C and X₇ is G.
 6. The immunostimulatory oligonucleotide of claim 1 having about 14 to 40 nucleotides.
 7. The immunostimulatory oligonucleotide of claim 1 having a modified phosphate backbone.
 8. The immunostimulatory oligonucleotide of claim 7 wherein the modification is on the 5′ inter-nucleotide linkages.
 9. The immunostimulatory oligonucleotide of claim 7 wherein the backbone modification is on the 3′ inter-nucleotide linkages.
 10. The immunostimulatory oligonucleotide of claim 1 comprising internucleotide linkages wherein at least one of the linkages is a phosphorothioate linkage.
 11. The immunostimulatory oligonucleotide of claim 1, having a sequence comprising: 5′-N X₁X₂X₃X₄X₅X₆X₇X₈ N-3′ wherein N is an oligonucleotide composed of about 3-25 nucleotides.
 12. The immunostimulatory oligonucleotide of claim 11, having a sequence comprising: 5′-NTTTT(G/C)TN-3′
 13. The immunostimulatory oligonucleotide of claim 1 which consists of a nucleotide sequence selected from the group consisting of: TGCTGCTTTTGTGCTTTTGTGCTT (SEQ ID No 1); TCATCATTTTGTCATTTTGTCATT (SEQ ID No 2); TCCTCCTTTTGTCCTTTTGTCCTT (SEQ ID No 3); TCTTCTTTTTGTCTTTTTGTCTTT (SEQ ID No 4); TAGTAGTTTTGTAGTTTTGTAGTT (SEQ ID No 5); TGGTGGTTTTGTGGTTTTGTGGTT (SEQ ID No 6); TTGTTGTTTTGTTGTTTTGTTGTT (SEQ ID No 7); TCATTTTTTTGTTTTTTTGTCATT (SEQ ID No 10); TCATTGTTTTGTTGTTTTGTCATT (SEQ ID No 11); TCATTCTTTTGTTCTTTTGTCATT (SEQ ID No 12); TCATAATTTTGTAATTTTGTCATT (SEQ ID No 14); TCATTATTTTGTTATTTTGTCATT (SEQ ID No 15); TCATGATTTTGTGATTTTGTCATT (SEQ ID No 16); TCATCCTTTTGTCCTTTTGTCATT (SEQ ID No 17); TCATCTTTTTGTCTTTTTGTCATT (SEQ ID No 18); CATTTTGTTTTTTTTTTTTTTTTT (SEQ ID No 20); TTCATTTTGTTTTTTTTTTTTTTT (SEQ ID No 21); TTTTCATTTTGTTTTTTTTTTTTT (SEQ ID No 22); TTTTTTCATTTTGTTTTTTTTTTT (SEQ ID No 23); TTTTTTTTCATTTTGTTTTTTTTT (SEQ ID No 24); TTTTTTTTTTCATTTTGTTTTTTT (SEQ ID No 25); TTTTTTTTTTTTCATTTTGTTTTT (SEQ ID No 26); TTTTTTTTTTTTTTCATTTTGTTT (SEQ ID No 27); TTTTTTTTTTTTTTTTCATTTTGT (SEQ ID No 28); TTTTCATTTTGTCATTTTGTTTTT (SEQ ID No 29); TCATCAATTTGTCAATTTGTCATT (SEQ ID No 30); TCATCATATTGTCATATTGTCATT (SEQ ID No 31); TCATCATTATGTCATTATGTCATT (SEQ ID No 32); TCATCATTTAGTCATTTAGTCATT (SEQ ID No 33); TCATCATTTTATCATTTTATCATT (SEQ ID No 34); TCATCATTTTTTCATTTTTTCATT (SEQ ID No 35); TCATCATTTTCTCATTTTCTCATT (SEQ ID No 36); TCATCATTTTGACATTTTGACATT (SEQ ID No 37); TCATCATTTAGACATTTAGACATT (SEQ ID No 38); TCATCATTATGACATTATGACATT (SEQ ID No 39); TCATCATATTGACATATTGACATT (SEQ ID No 40); ACATCATTTTGTCATTTTGTCATT (SEQ ID No 46); CCATCATTTTGTCATTTTGTCATT (SEQ ID No 47); GCATCATTTTGTCATTTTGTCATT (SEQ ID No 48); TAATCATTTTGTCATTTTGTCATT (SEQ ID No 49); TTATCATTTTGTCATTTTGTCATT (SEQ ID No 50); TGATCATTTTGTCATTTTGTCATT (SEQ ID No 51); TCCTCATTTTGTCATTTTGTCATT (SEQ ID No 52); TCTTCATTTTGTCATTTTGTCATT (SEQ ID No 53); TCGTCATTTTGTCATTTTGTCATT (SEQ ID No 54); TCAACATTTTGTCATTTTGTCATT (SEQ ID No 55); TCACCATTTTGTCATTTTGTCATT (SEQ ID No 56); TCAGCATTTTGTCATTTTGTCATT (SEQ ID No 57); TCATCATTTTGTCATTTTGTAATT (SEQ ID No 58); TCATCATTTTGTCATTTTGTTATT (SEQ ID No 59); TCATCATTTTGTCATTTTGTGATT (SEQ ID No 60); TCATCATTTTGTCATTTTGTCCTT (SEQ ID No 61); TCATCATTTTGTCATTTTGTCTTT (SEQ ID No 62); TCATCATTTTGTCATTTTGTCGTT (SEQ ID No 63); TCATCATTTTGTCATTTTGTCAAT (SEQ ID No 64); TCATCATTTTGTCATTTTGTCACT (SEQ ID No 65); TCATCATTTTGTCATTTTGTCAGT (SEQ ID No 66); TCATCATTTTGTCATTTTGTCATA (SEQ ID No 67); TCATCATTTTGTCATTTTGTCATC (SEQ ID No 68); TCATCATTTTGTCATTTTGTCATG (SEQ ID No 69); TTTTCATTTTGTTTTT (SEQ ID No 71); TTTTCATTTTGTTTTTTTTT (SEQ ID No 72); TTTTTTTTTTTTCATTTTGTTTTT (SEQ ID No 73); TTTTCATTTTGTTTTTTTTTTTTTTTTT (SEQ ID No 74).
 14. An immunostimulatory oligonucleotide which contains a nucleotide sequence selected from the group consisting of: TGCTGCTTTTGTGCTTTTGTGCTT (SEQ ID No 1); TCATCATTTTGTCATTTTGTCATT (SEQ ID No 2); TCCTCCTTTTGTCCTTTTGTCCTT (SEQ ID No 3); TCTTCTTTTTGTCTTTTTGTCTTT (SEQ ID No 4); TAGTAGTTTTGTAGTTTTGTAGTT (SEQ ID No 5); TGGTGGTTTTGTGGTTTTGTGGTT (SEQ ID No 6); TTGTTGTTTTGTTGTTTTGTTGTT (SEQ ID No 7); TCATTTTTTTGTTTTTTTGTCATT (SEQ ID No 10); TCATTGTTTTGTTGTTTTGTCATT (SEQ ID No 11); TCATTCTTTTGTTCTTTTGTCATT (SEQ ID No 12); TCATAATTTTGTAATTTTGTCATT (SEQ ID No 14); TCATTATTTTGTTATTTTGTCATT (SEQ ID No 15); TCATGATTTTGTGATTTTGTCATT (SEQ ID No 16); TCATCCTTTTGTCCTTTTGTCATT (SEQ ID No 17); TCATCTTTTTGTCTTTTTGTCATT (SEQ ID No 18); CATTTTGTTTTTTTTTTTTTTTTT (SEQ ID No 20); TTCATTTTGTTTTTTTTTTTTTTT (SEQ ID No 21); TTTTCATTTTGTTTTTTTTTTTTT (SEQ ID No 22); TTTTTTCATTTTGTTTTTTTTTTT (SEQ ID No 23); TTTTTTTTCATTTTGTTTTTTTTT (SEQ ID No 24); TTTTTTTTTTCATTTTGTTTTTTT (SEQ ID No 25); TTTTTTTTTTTTCATTTTGTTTTT (SEQ ID No 26); TTTTTTTTTTTTTTCATTTTGTTT (SEQ ID No 27); TTTTTTTTTTTTTTTTCATTTTGT (SEQ ID No 28); TTTTCATTTTGTCATTTTGTTTTT (SEQ ID No 29); TCATCAATTTGTCAATTTGTCATT (SEQ ID No 30); TCATCATATTGTCATATTGTCATT (SEQ ID No 31); TCATCATTATGTCATTATGTCATT (SEQ ID No 32); TCATCATTTAGTCATTTAGTCATT (SEQ ID No 33); TCATCATTTTATCATTTTATCATT (SEQ ID No 34); TCATCATTTTTTCATTTTTTCATT (SEQ ID No 35); TCATCATTTTCTCATTTTCTCATT (SEQ ID No 36); TCATCATTTTGACATTTTGACATT (SEQ ID No 37); TCATCATTTAGACATTTAGACATT (SEQ ID No 38); TCATCATTATGACATTATGACATT (SEQ ID No 39); TCATCATATTGACATATTGACATT (SEQ ID No 40); ACATCATTTTGTCATTTTGTCATT (SEQ ID No 46); CCATCATTTTGTCATTTTGTCATT (SEQ ID No 47); GCATCATTTTGTCATTTTGTCATT (SEQ ID No 48); TAATCATTTTGTCATTTTGTCATT (SEQ ID No 49); TTATCATTTTGTCATTTTGTCATT (SEQ ID No 50); TGATCATTTTGTCATTTTGTCATT (SEQ ID No 51); TCCTCATTTTGTCATTTTGTCATT (SEQ ID No 52); TCTTCATTTTGTCATTTTGTCATT (SEQ ID No 53); TCGTCATTTTGTCATTTTGTCATT (SEQ ID No 54); TCAACATTTTGTCATTTTGTCATT (SEQ ID No 55); TCACCATTTTGTCATTTTGTCATT (SEQ ID No 56); TCAGCATTTTGTCATTTTGTCATT (SEQ ID No 57); TCATCATTTTGTCATTTTGTAATT (SEQ ID No 58); TCATCATTTTGTCATTTTGTTATT (SEQ ID No 59); TCATCATTTTGTCATTTTGTGATT (SEQ ID No 60); TCATCATTTTGTCATTTTGTCCTT (SEQ ID No 61); TCATCATTTTGTCATTTTGTCTTT (SEQ ID No 62); TCATCATTTTGTCATTTTGTCGTT (SEQ ID No 63); TCATCATTTTGTCATTTTGTCAAT (SEQ ID No 64); TCATCATTTTGTCATTTTGTCACT (SEQ ID No 65); TCATCATTTTGTCATTTTGTCAGT (SEQ ID No 66); TCATCATTTTGTCATTTTGTCATA (SEQ ID No 67); TCATCATTTTGTCATTTTGTCATC (SEQ ID No 68); TCATCATTTTGTCATTTTGTCATG (SEQ ID No 69); TTTTCATTTTGTTTTT (SEQ ID No 71); TTTTCATTTTGTTTTTTTTT (SEQ ID No 72); TTTTTTTTTTTTCATTTTGTTTTT (SEQ ID No 73); TTTTCATTTTGTTTTTTTTTTTTTTTTT (SEQ ID No 74).
 15. The immunostimulatory oligonucleotide of claim 1 wherein the immunostimulatory oligonucleotide is encapsulated in a slow release delivery vehicle
 16. The immunostimulatory oligonucleotide of claim 1 wherein the immunostimulatory oligonucleotide is included in a pharmaceuticallly acceptable carrier.
 17. A composition comprising an immunostimulatory oligonucleotide according to claim 1 and a pharmaceutically acceptable carrier.
 18. A composition according to claim 17 wherein said immunostimulatory oligonucleotide is included in a plasmid.
 19. A composition according to claim 17 further comprising an antigen.
 20. A composition according to claim 19 wherein the antigen is selected from the group consisting of viruses, bacteria, fungi, parasites, tumoral cells, toxins, allergens, proteins, glycolipids and polysaccharides.
 21. A composition according to claim 19 wherein the antigen is a viral antigen, a bacterial antigen, a human or animal tumor cell and/or a fungal antigen.
 22. A composition according to claim 17 further comprising a plasmid encoding an antigen.
 23. A method for inducing B-cell activation in a subject in need of such activation comprising administering to the subject an effective amount of an immunostimulatory oligonucleotide of claim
 1. 24. The method of claim 23, wherein the subject is a human.
 25. The method of claim 23 wherein the immunostimulatory oligonucleotide is encapsulated in a slow release delivery vehicle.
 26. The method of claim 23 wherein the immunostimulatory oligonucleotide is included in a pharmaceutical composition comprising a pharmaceutically acceptable carrier.
 27. The method of claim 23 wherein the administration comprises contacting the subject's B cells with an effective amount of the oligonucleotide.
 28. The method of claim 23 wherein the amount is effective for treating, preventing or ameliorating an immune system disorder in said subject.
 29. The method of claim 23 wherein the amount is effective for treating, preventing or ameliorating a tumoral disease in said subject.
 30. A method for treating, preventing or ameliorating a tumoral disease in a subject comprising the steps of: (a) contacting white blood cells obtained from the subject with an effective amount of an immunostimulatory oligonucleotide of claim 1, ex vivo, thereby producing activated B lymphocytes; and (b) readministering the activated white blood cells obtained in step a) to the subject.
 31. The method of claim 23 wherein the oligonucleotide is administered to a subject together with a vaccine.
 32. The method of claim 23 wherein the oligonucleotide has been conjugated with one or more antigens.
 33. The method of claim 23 wherein the oligonucleotide is administered as an adjuvant in a vaccine composition comprising at least one antigen.
 34. The method of claim 33 wherein the oligonucleotide is administered to the subject contemporaneously or simultaneously with a vaccine comprising at least one antigen.
 35. The method of claim 34 wherein the subject is vaccinated prophylactically or therapeutically.
 36. The method of claim 33 wherein the oligonucleotide is present in the composition in amounts within the range from 10 to 10,000 μg per dose.
 37. The method of claim 23 wherein the oligonucleotide is used as an adjuvant in a vaccine composition selected from the group consisting of liquid vaccine formulations and lyophilized vaccine formulations.
 38. A method of vaccination of a subject where the immunostimulatory oligonucleotide of claim 1 and an antigen are administered to the subject by intramuscular injection at the same site.
 39. The method of claim 38 wherein the subject is vaccinated prophylactically or therapeutically.
 40. A method of vaccination of a subject where the oligonucleotide of claim 1 and the antigen are administered by the oral, intranasal, anal, vaginal, transdermic or mucosal route.
 41. The method of claim 40 wherein the subject is vaccinated prophylactically or therapeutically.
 42. A method for inducing plasmacytoid dendritic cell activation in a subject in need of such activation comprising administering to the subject an effective amount of an immunostimulatory oligonucleotide of claim
 1. 43. The method of claim 42, wherein the subject is a human.
 44. The method of claim 42 wherein the immunostimulatory oligonucleotide is encapsulated in a slow release delivery vehicle.
 45. The method of claim 42 wherein the immunostimulatory oligonucleotide is included in a pharmaceutical composition comprising a pharmaceutically acceptable carrier.
 46. The method of claim 42 comprising contacting the subject's plasmacytoid dendritic cells with an effective amount of the oligonucleotide.
 47. The method of claim 42 wherein the amount is effective for treating, preventing or ameliorating an immune system disorder in the subject.
 48. The method of claim 42 wherein the amount is effective for treating, preventing or ameliorating a tumoral disease in the subject.
 49. The method of claim 42 comprising the steps of: (a) contacting white blood cells obtained from the subject with an effective amount of an immunostimulatory oligonucleotide of claim 1, ex vivo, thereby producing activated plasmacytoid dendritic cells; and (b) readministering the activated white blood cells obtained in step a) to the subject.
 50. The method of claim 42 wherein the oligonucleotide is administered to a subject together with a vaccine.
 51. The method of claim 42 wherein the oligonucleotide has been conjugated with one or more antigens.
 52. The method of claim 42 wherein the oligonucleotide is administered as an adjuvant in a vaccine composition comprising at least one antigen.
 53. The method of claim 42 wherein the oligonucleotide is administered contemporaneously or simultaneously with an antigen.
 54. The method of claim 52 wherein the subject is vaccinated prophylactically or therapeutically.
 55. The method of claim 52 wherein the oligonucleotide is present in said composition in amounts of from 10 to 10,000 μg per dose.
 56. The method of claim 52 wherein the vaccine composition is selected from the group consisting of liquid vaccine formulations and lyophilized vaccine formulations.
 57. The method of claim 53 wherein the immunostimulatory oligonucleotide of claim 1 and the antigen are administered to the subject by intramuscular injection at the same site.
 58. T he method of claim 53 wherein the oligonucleotide of claim 1 and the antigen are administered by the oral, intranasal, anal, vaginal, transdermic or mucosal route.
 59. The method of claim 58 wherein the subject is vaccinated prophylactically or therapeutically.
 60. The method of claim 14, wherein the oligonucleotide has about 14 to about 58 nucleotides
 61. The method of claim 1, wherein the remaining two of X₃X₄X₅X₆ and X₈ are C,T,G,A or absent. 